Al-Jibori, Subhi A. et al. published their research in Polyhedron in 2022 | CAS: 13820-53-6

Sodium tetrachloropalladate(II) (cas: 13820-53-6) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.COA of Formula: Cl4Na2Pd

Palladium(II) 2-mercaptobenzamide (o-SC6H4CONH2) complexes: Crystal structure of trans-[Pd(o-SC6H4CONH2)2(PPh3)2] was written by Al-Jibori, Subhi A.;Al-Jibori, Ghassan H. H.;Saleh, Syran S.;Al-Janabi, Ahmed S. M.;Laguna, Mariano;Wagner, Christoph. And the article was included in Polyhedron in 2022.COA of Formula: Cl4Na2Pd The following contents are mentioned in the article:

The reaction of [Hg(mbm)2] (mbm = o-SC6H4CONH2) with Na2S releases Na[mbm] which reacts with Pd(II) salts to give [Pd(mbm)2]. While its precise mol. structure is unknown, [Pd(mbm)2] reacts with two equivalent of PPh3 to afford trans-[Pd(κ1-mbm)2(PPh3)2] in which the mbm ligands bind through a sulfur atom. With dppf, a similar complex, [Pd(κ1-mbm)22-dppf)], is formulated with the mbm ligands being forced into a relative cis orientation. With dppm, a mixture of mononuclear [Pd(κ1-mbm)2(dppm)] and binuclear [Pd(κ1-mbm)2(μ-dppm)]2 results. The new complexes have been characterized by IR, 1H and 31P{1H} NMR, molar conductivity and elemental anal., and in addition, the mol. structure of trans-[Pd(κ2-mbm)2(PPh3)2] was confirmed by x-ray diffraction. This study involved multiple reactions and reactants, such as Sodium tetrachloropalladate(II) (cas: 13820-53-6COA of Formula: Cl4Na2Pd).

Sodium tetrachloropalladate(II) (cas: 13820-53-6) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.COA of Formula: Cl4Na2Pd

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Schlindwein, Simon H. et al. published their research in European Journal of Inorganic Chemistry in 2021 | CAS: 75-57-0

Tetramethylammonium chloride (cas: 75-57-0) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Category: chlorides-buliding-blocks

Small Variations, Big Impact: Structural Diversity of the Complexes of a Phosphane-Decorated Benzenedithiol with Group-11 Metals was written by Schlindwein, Simon H.;Nieger, Martin;Gudat, Dietrich. And the article was included in European Journal of Inorganic Chemistry in 2021.Category: chlorides-buliding-blocks The following contents are mentioned in the article:

Reaction of a phosphine-decorated benzenedithiol (pbdtH2) with coinage metal salts furnished polynuclear complexes [M2(pbdtH)2] (M = AuI) or [cat][M5(pbdt)3] (cat = unipos. cation, M = AgI, CuI), which were characterized by anal. and spectroscopic techniques and single-crystal x-ray diffraction studies. Also, a double salt with an anion [Ag5(pbdt)3(PPh3)] that proved unstable in solution was characterized crystallog. The spectroscopic and crystallog. data revealed that the Cu(I) and Ag(I) complexes exhibit, despite their like stoichiometric composition, isomeric mol. structures. The observed disparities were reproduced by DFT studies. The dinuclear Au(I) complex was found to undergo air-oxidation to furnish a mixed-valent complex [(AuIII)2(AuI)2(pbdt)4]. The copper(I) – but not the isomeric silver(I) complexes – showed luminescence in the solid state. This study involved multiple reactions and reactants, such as Tetramethylammonium chloride (cas: 75-57-0Category: chlorides-buliding-blocks).

Tetramethylammonium chloride (cas: 75-57-0) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Category: chlorides-buliding-blocks

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Singh, Priyanka et al. published their research in ChemistrySelect in 2021 | CAS: 5137-55-3

N-Methyl-N,N-dioctyloctan-1-aminium chloride (cas: 5137-55-3) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Application of 5137-55-3

Synergistic Effect of Iodide Ion and N-methyl-N,N,N-trioctylammonium Chloride on Corrosion Inhibition of Carbon Steel in 0.5 M H2SO4: Experimental and Computational Approach was written by Singh, Priyanka;Singh Chauhan, Dheeraj;Singh Chauhan, Sampat;Ahmad Quraishi, Mumtaz;Swarupa Tripathy, Sushree. And the article was included in ChemistrySelect in 2021.Application of 5137-55-3 The following contents are mentioned in the article:

An ionic liquid Aliquat 336 was for the first time analyzed for its adsorption and corrosion inhibition behavior for carbon steel surface in 0.5 M H2SO4. The inhibition performance was studied using gravimetric and electrochem. techniques supported by surface anal. measurements. The inhibitor exerted an efficiency of 96.53% at 12×10-6 M. Significant improvement was achieved with iodide ions, which at 3.01×10-4 M, produced a remarkable rise in the efficiency to 99.03%. The adsorption of the inhibitor on the metallic surface followed the Langmuir isotherm at 298 K in the concentration range of 2.47 to 12.37×10-6 M. Polarization studies indicated a mixed-mode of inhibitor action with the cathodic predominance. The SEM studies showed a smooth metal surface in contact with the inhibitor, and a representative decrease in surface roughness was observed by AFM studies. Monte Carlo simulations showed inhibitor adsorption in a flat orientation on the metal surface with high adsorption energy. This study involved multiple reactions and reactants, such as N-Methyl-N,N-dioctyloctan-1-aminium chloride (cas: 5137-55-3Application of 5137-55-3).

N-Methyl-N,N-dioctyloctan-1-aminium chloride (cas: 5137-55-3) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Application of 5137-55-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Singh, Akhil Pratap et al. published their research in Physical Chemistry Chemical Physics in 2017 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Reference of 122-18-9

Enhanced stability and water solubilizing capacity of water-in-oil microemulsions based on protic ionic liquids was written by Singh, Akhil Pratap;Kundu, Kaushik;Singh, Vikram;Gardas, Ramesh L.;Senapati, Sanjib. And the article was included in Physical Chemistry Chemical Physics in 2017.Reference of 122-18-9 The following contents are mentioned in the article:

To increase the stability and water uptake capacity of water-in-oil (W/O) microemulsions, the physicochem. behavior of a series of W/O microemulsion-based protic ionic liquids was assessed, wherein solute amounts of biocompatible tetramethylguanidinium cation-based ionic liquids (IL) were added to the W/O microemulsion aqueous phases. Fourier transform IR (FTIR) spectroscopy and time-resolved fluorescence measurements showed increased water uptake by these reverse micellar droplets vs. conventional W/O microemulsions with similar compositions Dynamic light scattering and differential scanning calorimetry measurements suggested greater droplet thermal stability in the presence of IL. NMR and FTIR measurements and ab-initio calculations explained these results by showing an extended H bonding network between interfacial water and protic IL ions, and strong electrostatic associations between surfactant head-groups and IL anions. Results provide potential applications of protic ionic liquids in emulsion and microemulsion science and technol. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Reference of 122-18-9).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Reference of 122-18-9

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Lastra, Lauren S. et al. published their research in Nature Communications in 2022 | CAS: 7447-41-8

Lithium chloride (cas: 7447-41-8) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Application In Synthesis of Lithium chloride

On the origins of conductive pulse sensing inside a nanopore was written by Lastra, Lauren S.;Bandara, Y. M. Nuwan D. Y.;Nguyen, Michelle;Farajpour, Nasim;Freedman, Kevin J.. And the article was included in Nature Communications in 2022.Application In Synthesis of Lithium chloride The following contents are mentioned in the article:

Nanopore sensing is nearly synonymous with resistive pulse sensing due to the characteristic occlusion of ions during pore occupancy, particularly at high salt concentrations Contrarily, conductive pulses are observed under low salt conditions wherein electroosmotic flow is significant. Most literature reports counterions as the dominant mechanism of conductive events (a mol.-centric theory). However, the counterion theory does not fit well with conductive events occurring via net neutral-charged protein translocation, prompting further investigation into translocation mechanics. Herein, we demonstrate theory and experiments underpinning the translocation mechanism (i.e., electroosmosis or electrophoresis), pulse direction (i.e., conductive or resistive) and shape (e.g., monophasic or biphasic) through fine control of chem., phys., and electronic parameters. Results from these studies predict strong electroosmosis plays a role in driving DNA events and generating conductive events due to polarization effects (i.e., a pore-centric theory). This study involved multiple reactions and reactants, such as Lithium chloride (cas: 7447-41-8Application In Synthesis of Lithium chloride).

Lithium chloride (cas: 7447-41-8) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Application In Synthesis of Lithium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Pallesen, Jakob S. et al. published their research in Journal of Medicinal Chemistry in 2021 | CAS: 638-07-3

Ethyl 4-chloro-3-oxobutanoate (cas: 638-07-3) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Recommanded Product: 638-07-3

Deconstructing Noncovalent Kelch-like ECH-Associated Protein 1 (Keap1) Inhibitors into Fragments to Reconstruct New Potent Compounds was written by Pallesen, Jakob S.;Narayanan, Dilip;Tran, Kim T.;Solbak, Sara M. Oe.;Marseglia, Giuseppe;Soerensen, Louis M. E.;Hoej, Lars J.;Munafo, Federico;Carmona, Rosa M. C.;Garcia, Anthony D.;Desu, Haritha L.;Brambilla, Roberta;Johansen, Tommy N.;Popowicz, Grzegorz M.;Sattler, Michael;Gajhede, Michael;Bach, Anders. And the article was included in Journal of Medicinal Chemistry in 2021.Recommanded Product: 638-07-3 The following contents are mentioned in the article:

Targeting the protein-protein interaction (PPI) between nuclear factor erythroid 2-related factor 2 (Nrf2) and Kelch-like ECH-associated protein 1 (Keap1) is a potential therapeutic strategy to control diseases involving oxidative stress. Here, six classes of known small-mol. Keap1-Nrf2 PPI inhibitors were dissected into 77 fragments in a fragment-based deconstruction reconstruction (FBDR) study and tested in four orthogonal assays. This gave 17 fragment hits of which six were shown by X-ray crystallog. to bind in the Keap1 Kelch binding pocket. Two hits were merged into pyrazole I with a 220-380-fold stronger affinity (Ki = 16μM) relative to the parent fragments. Systematic optimization resulted in several novel analogs with Ki values of 0.04-0.5μM, binding modes determined by X-ray crystallog., and enhanced microsomal stability. This demonstrates how FBDR can be used to find new fragment hits, elucidate important ligand-protein interactions, and identify new potent inhibitors of the Keap1-Nrf2 PPI. This study involved multiple reactions and reactants, such as Ethyl 4-chloro-3-oxobutanoate (cas: 638-07-3Recommanded Product: 638-07-3).

Ethyl 4-chloro-3-oxobutanoate (cas: 638-07-3) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Recommanded Product: 638-07-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Kokan, Zoran et al. published their research in Chem in 2021 | CAS: 75-57-0

Tetramethylammonium chloride (cas: 75-57-0) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.COA of Formula: C4H12ClN

Supramolecular hydrogelation via host-guest anion recognition: Lamellar hydrogel materials for the release of cationic cargo was written by Kokan, Zoran;Duskova-Smrckova, Miroslava;Sindelar, Vladimir. And the article was included in Chem in 2021.COA of Formula: C4H12ClN The following contents are mentioned in the article:

Hydrogelation triggered by host-guest anion recognition is difficult to achieve due to the challenging anion recognition in water and de novo gelator design. Herein, we report such a hydrogel system, based on bambus[6]uril anion receptor, BU. Albeit not a gelator per se, BU formed hydrogels selectively in the presence of iodides or perchlorates. Anion recognition by BU governed the hydrogelation, indicated by the NMR, ATR-IR, and single-crystal X-ray. Gelation mechanism and lamellar nature of the network structure were elucidated by SAXS, cryoSEM, and holotomog. methods. Rheol. characterization revealed the hydrogels were stable and relatively strong. In physiol. saline solutions, the hydrogels released cationic cargo by cation metathesis, leading to a gel-to-gel transformation. Choline derivatives, as model drugs, exhibited slow release from the hydrogels. Our simple hydrogel system may inspire the design of smart materials based on host-guest anion recognition, where the release or sequestration of specific charged species are desirable. This study involved multiple reactions and reactants, such as Tetramethylammonium chloride (cas: 75-57-0COA of Formula: C4H12ClN).

Tetramethylammonium chloride (cas: 75-57-0) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.COA of Formula: C4H12ClN

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Li, Zhijun et al. published their research in Applied Catalysis, B: Environmental in 2022 | CAS: 13820-53-6

Sodium tetrachloropalladate(II) (cas: 13820-53-6) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Quality Control of Sodium tetrachloropalladate(II)

Strong electronic interaction of indium oxide with palladium single atoms induced by quenching toward enhanced hydrogenation of nitrobenzene was written by Li, Zhijun;Zhang, Mingyang;Dong, Xiuli;Ji, Siqi;Zhang, Lili;Leng, Leipeng;Li, Honghong;Horton, J. Hugh;Xu, Qian;Zhu, Junfa. And the article was included in Applied Catalysis, B: Environmental in 2022.Quality Control of Sodium tetrachloropalladate(II) The following contents are mentioned in the article:

The realization of efficient and fully controllable synthesis of single atom catalysts is an exciting frontier, yet still challenging in the modern catalysis field. Here we describe a straightforward high-temperature quenching approach to precisely construct isolated palladium atoms supported over cubic indium oxide, with individual palladium atoms coordinated with four neighboring oxygen atoms. This palladium catalyst achieves exceptional catalytic efficiency in the selective hydrogenation of nitrobenzene to aniline, with more than 99% chemoselectivity under almost 100% conversion. Moreover, it delivers excellent recyclability, anti-CO poisoning ability, storage stability, and substrate tolerance. DFT calculations further reveal that the high catalytic activity stems from the optimized electronic structure and the charge states of palladium atoms in the defect-containing indium oxide. Our findings provide an effective approach to engineering single atom catalysts at the at. level and open the door to a wide variety of catalytic reactions. This study involved multiple reactions and reactants, such as Sodium tetrachloropalladate(II) (cas: 13820-53-6Quality Control of Sodium tetrachloropalladate(II)).

Sodium tetrachloropalladate(II) (cas: 13820-53-6) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Quality Control of Sodium tetrachloropalladate(II)

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Zhou, Hancheng et al. published their research in Bioresource Technology in 2011 | CAS: 6294-17-3

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Application of 6294-17-3

Enhanced performance of lipase-catalyzed kinetic resolution of secondary alcohols in monoether-functionalized ionic liquids was written by Zhou, Hancheng;Chen, Jin;Ye, Linmin;Lin, Haiqiang;Yuan, Youzhu. And the article was included in Bioresource Technology in 2011.Application of 6294-17-3 The following contents are mentioned in the article:

Several cationic monoether-functionalized ionic liquids (MEF-ILs) with different substituents were synthesized and used as media for kinetic resolution of secondary alcs. catalyzed by several lipases. The results indicate that Novozym 435 (an immobilized Candida antarctica Lipase B) had higher efficiency compared to other lipases in deracemization. The alkyl substituents at the 2- and 3-positions in the imidazolium ring of MEF-ILs were found to contribute to the increased enantioselectivity and enhancement of the reaction rate, resp., while the higher stereo-hindrance of ether bonds decreased the activity. An enantioselectivity higher than 99% with 50% conversion of rac-1-phenylethanol was achieved using the catalyst system comprised of Novozym 435 and the MEF-IL 1-(3-ethoxypropyl)-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)imide. The catalytic system could be separated and reused without considerable activity loss. MEF-ILs can be a new class of enzyme-benign media suitable for lipase-catalyzed kinetic resolution of secondary alcs. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Application of 6294-17-3).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Application of 6294-17-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Raghuvanshi, Ashutosh et al. published their research in Molecular and Cellular Endocrinology in 2017 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.HPLC of Formula: 95-88-5

3-Piperidylethoxypterocarpan: A potential bone anabolic agent that improves bone quality and restores trabecular micro-architecture in ovariectomized osteopenic rats was written by Raghuvanshi, Ashutosh;Kumar, Amit;Tyagi, Abdul M.;Kureel, Jyoti;Awasthi, Pallavi;Purohit, Deepak;Mansoori, Mohd. Nizam;Shukla, Priyanka;Srivastava, Kamini;Gautam, Abnish K.;Saxena, Ruchi;Dwivedi, Anila;Singh, Divya;Goel, Atul. And the article was included in Molecular and Cellular Endocrinology in 2017.HPLC of Formula: 95-88-5 The following contents are mentioned in the article:

A series of new 6H-benzofuro[3, 2-c]chromenes (BFC, pterocarpans) with structure-activity relationships were investigated for their potential use in osteoporosis treatment. One of the BFCs 3-piperidylethoxypterocarpan 20 promotes osteoblast differentiation and mineralization at a dose as low as 1 pM via activation of ER/P38MAPK/BMP-2 pathway. When evaluated for in-vivo osteogenic activity in female Sprague-Dawley rats, BFC 20 increased bone mineral d. and new bone formation, compared with control at 1.0 and 10.0 mg/kg/body weight by oral gavage for 30 days. The compound was devoid of any uterotrophic effect and led to the new bone formation in adult ovariectomized osteopenic rats. BFC 20 compound also inhibited bone resorption by reducing Ovx induced increase in urinary CTx, thus exhibiting both bone anabolic and anti-catabolic action. Finally, BFC 20 treatment to Ovx rats led to improved trabecular microarchitectural restoration and exhibited therapeutic potential as a dual acting anti-osteoporotic agent for the management of osteoporosis. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5HPLC of Formula: 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.HPLC of Formula: 95-88-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics