Spicer, Julie A. et al. published their research in European Journal of Medicinal Chemistry in 2017 | CAS: 777-44-6

3-(Trifluoromethyl)benzene-1-sulfonyl chloride (cas: 777-44-6) 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.Recommanded Product: 3-(Trifluoromethyl)benzene-1-sulfonyl chloride

Substituted arylsulphonamides as inhibitors of perforin-mediated lysis was written by Spicer, Julie A.;Miller, Christian K.;O’Connor, Patrick D.;Jose, Jiney;Huttunen, Kristiina M.;Jaiswal, Jagdish K.;Denny, William A.;Akhlaghi, Hedieh;Browne, Kylie A.;Trapani, Joseph A.. And the article was included in European Journal of Medicinal Chemistry in 2017.Recommanded Product: 3-(Trifluoromethyl)benzene-1-sulfonyl chloride This article mentions the following:

The structure-activity relationships for a series of arylsulfonamide-based inhibitors of the pore-forming protein perforin have been explored. Perforin is a key component of the human immune response, however, inappropriate activity has also been implicated in certain auto-immune and therapy-induced conditions such as allograft rejection and graft vs. host disease. Since perforin is expressed exclusively by cells of the immune system, inhibition of this protein would be a highly selective strategy for the immunosuppressive treatment of these disorders. Compounds from this series were demonstrated to be potent inhibitors of the lytic action of both isolated recombinant perforin and perforin secreted by natural killer cells in vitro. Several potent and soluble examples were assessed for in vivo pharmacokinetic properties and found to be suitable for progression to an in vivo model of transplant rejection. In the experiment, the researchers used many compounds, for example, 3-(Trifluoromethyl)benzene-1-sulfonyl chloride (cas: 777-44-6Recommanded Product: 3-(Trifluoromethyl)benzene-1-sulfonyl chloride).

3-(Trifluoromethyl)benzene-1-sulfonyl chloride (cas: 777-44-6) 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.Recommanded Product: 3-(Trifluoromethyl)benzene-1-sulfonyl chloride

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

Moi, Davide et al. published their research in Molecules in 2022 | CAS: 6590-96-1

2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1) 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Related Products of 6590-96-1

Synthesis of Sulfonamides Incorporating Piperidinyl-Hydrazidoureido and Piperidinyl-Hydrazidothioureido Moieties and Their Carbonic Anhydrase I, II, IX and XII Inhibitory Activity was written by Moi, Davide;Deplano, Alessandro;Angeli, Andrea;Balboni, Gianfranco;Supuran, Claudiu T.;Onnis, Valentina. And the article was included in Molecules in 2022.Related Products of 6590-96-1 This article mentions the following:

Here, we report a small library of hydrazinocarbonyl-ureido and -thioureido benzenesulfonamide derivatives, I [R = Ph, C6H11, PhCH2, etc., X = O, S], that were designed and synthesized as potent and selective human carbonic anhydrase inhibitors (hCAIs). The synthesized compounds were ev=aluated against isoforms hCA I, II, IX and XII using acetazolamide (AAZ) as standard inhibitor. Several urea and thiourea derivatives showed inhibitory activity at low nanomolar levels with selectivity against the cytosolic hCA II isoform, as well as the transmembrane, tumor-associated enzymes hCA IX and XII. The thiourea derivatives showed enhanced potency as compared to urea analogs. Addnl., eight compounds, I [R = 3-FC6H4, 2,6-Me2C6H3, 2-MeOC6H4, 4-MeOC6H4, X = O, S], were selected for docking anal. on isoform I, II, IX, XII to illustrate the potential interaction with the enzyme to better understand the activity against the different isoforms. In the experiment, the researchers used many compounds, for example, 2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1Related Products of 6590-96-1).

2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1) 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Related Products of 6590-96-1

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

Chandrasekhar, S. et al. published their research in Tetrahedron Letters in 2000 | CAS: 18437-66-6

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) 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.Computed Properties of C11H14ClNO2

Direct conversion of azides to carbamates and sulfonamides using Fe/NH4Cl: effect of sonication was written by Chandrasekhar, S.;Narsihmulu, Ch.. And the article was included in Tetrahedron Letters in 2000.Computed Properties of C11H14ClNO2 This article mentions the following:

A simple, direct and effective conversion of azides to carbamates and sulfonamides is achieved using Fe/NH4Cl in MeOH. The influence of ultrasonication and direct application in solution-phase combinatorial chem. are also studied by developing a 6×4 matrix library. In the experiment, the researchers used many compounds, for example, tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6Computed Properties of C11H14ClNO2).

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) 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.Computed Properties of C11H14ClNO2

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

Kim, Jeum-Jong et al. published their research in Synlett in 2006 | CAS: 14070-51-0

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) 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. 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.COA of Formula: C7H4ClNO3S

Conversion of nucleophilic halides to electrophilic halides: efficient and selective halogenation of azinones, amides, and carbonyl compounds using metal halide/lead tetraacetate was written by Kim, Jeum-Jong;Kweon, Deok-Heon;Cho, Su-Dong;Kim, Ho-Kyun;Lee, Sang-Gyeong;Yoon, Yong-Jin. And the article was included in Synlett in 2006.COA of Formula: C7H4ClNO3S This article mentions the following:

AlCl3/Pb(OAc)4 and ZnBr2/Pb(OAc)4 are efficient electrophilic N- and α-C-halogenating agents. A variety of azinones, amides, and carbonyl compounds were chemoselectively and regioselectively N- or α-C-halogenated in good to excellent yield using AlCl3/Pb(OAc)4 or ZnBr2/Pb(OAc)4 in acetonitrile. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0COA of Formula: C7H4ClNO3S).

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) 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. 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.COA of Formula: C7H4ClNO3S

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

Isley, Nicholas A. et al. published their research in Green Chemistry in 2014 | CAS: 18437-66-6

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) 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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Computed Properties of C11H14ClNO2

Installation of protected ammonia equivalents onto aromatic & heteroaromatic rings in water enabled by micellar catalysis was written by Isley, Nicholas A.;Dobarco, Sebastian;Lipshutz, Bruce H.. And the article was included in Green Chemistry in 2014.Computed Properties of C11H14ClNO2 This article mentions the following:

A single set of conditions consisting of a palladium catalyst, a com. available ligand, and a base allow for several types of C-N bond constructions to be conducted in water with the aid of a com. available “designer” surfactant (TPGS-750-M). Products containing a protected NH2 group in the form of a carbamate, sulfonamide, or urea can be fashioned starting with aryl or heteroaryl bromides, iodides, and in some cases, chlorides, as substrates. Reaction temperatures are in the range of room temperature to, at most, 50 °C, and result in essentially full conversion and good isolated yields. E.g., in presence of allylpalladium chloride dimer, a ligand, and TPGS-750-M in water, amidation of 4-BrC6H4CO2Et with carbamate H2NCO2Et gave 99% I. In the experiment, the researchers used many compounds, for example, tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6Computed Properties of C11H14ClNO2).

tert-Butyl (4-chlorophenyl)carbamate (cas: 18437-66-6) 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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Computed Properties of C11H14ClNO2

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

Moosavi-Zare, Ahmad Reza et al. published their research in Organic Preparations and Procedures International in 2022 | CAS: 76-83-5

(Chloromethanetriyl)tribenzene (cas: 76-83-5) 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. 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.Category: chlorides-buliding-blocks

The Synthesis of gem-Bisamides Using a Carbocationic Catalytic System in Neutral Media was written by Moosavi-Zare, Ahmad Reza;Goudarziafshar, Hamid;Jalilian, Zahra;Hajilouie, Zahra. And the article was included in Organic Preparations and Procedures International in 2022.Category: chlorides-buliding-blocks This article mentions the following:

Synthesis of N,N’-alkylidene bisamides I (R1 = 2-Br, 4-F, 4-NO2, etc.; R2 = Me, Ph) using TrCl as a homogeneous organocatalyst in neutral media. The products were prepared in high yields in short reaction times. The low cost of trityl choride, com. availability of the catalyst, short reaction times and the avoidance of harsh acidic conditions are important advantages of this work. In the experiment, the researchers used many compounds, for example, (Chloromethanetriyl)tribenzene (cas: 76-83-5Category: chlorides-buliding-blocks).

(Chloromethanetriyl)tribenzene (cas: 76-83-5) 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. 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.Category: chlorides-buliding-blocks

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

McIntee, Olivia M. et al. published their research in Polymer in 2022 | CAS: 4422-95-1

Trimesoylchloride (cas: 4422-95-1) 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. 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.Product Details of 4422-95-1

Elastic modulus of polyamide thin films formed by molecular layer deposition was written by McIntee, Olivia M.;Welch, Brian C.;Greenberg, Alan R.;George, Steven M.;Bright, Victor M.. And the article was included in Polymer in 2022.Product Details of 4422-95-1 This article mentions the following:

Mol. layer deposition (MLD) is a gas-phase deposition technique that can create ultra-thin films with precisely controlled chem. composition and thickness by depositing one monolayer at a time. This makes MLD an attractive technol. for desalination membranes among other applications. Given its relatively recent development, little information has been reported regarding the properties of MLD thin films. We present the results of an initial mech. property study of MLD films with thicknesses ranging from �0 to 2000 nm. MLD was utilized to create crosslinked polyamide films grown using either m-phenylenediamine (MPD) and trimesoyl chloride (TMC) reactants or piperazine (PIP) and TMC reactants. The elastic modulus of the films was determined using at. force microscopy (AFM). The results show that the modulus was independent of film thickness with values of 4.36 ± 1.19 GPa and 5.24 ± 1.06 GPa for the MLD films grown using the MPD-TMC and PIP-TMC chemistries, resp. These values are of the same order of magnitude as those reported for much thicker polyamide films, but higher than the modulus of polyamide films fabricated using interfacial polymerization In the experiment, the researchers used many compounds, for example, Trimesoylchloride (cas: 4422-95-1Product Details of 4422-95-1).

Trimesoylchloride (cas: 4422-95-1) 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. 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.Product Details of 4422-95-1

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

Farook, N. A. Mohamed et al. published their research in Asian Journal of Chemistry in 2007 | CAS: 14070-51-0

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Product Details of 14070-51-0

Kinetics of oxidation of some amino acids by N-chlorosaccharin in aqueous acetic acid medium was written by Farook, N. A. Mohamed;Khan, T. Hidhayathulla;Dameem, G. A. Seyed. And the article was included in Asian Journal of Chemistry in 2007.Product Details of 14070-51-0 This article mentions the following:

The kinetics of oxidation of amino acids (AA), glycine, alanine, aspartic acid, arginine, and histidine, by N-chlorosaccharin (NCSA) in aqueous acetic acid medium in the presence of perchloric acid have been investigated. The observed rate of oxidation is first order in [AA], [NCSA] and of inverse functional order in [H+]. The main product of the oxidation is the corresponding aldehyde. The ionic strength on the reaction rate has no significant effect. The effect of changing the dielec. constant of the medium on the rate indicates the reaction to be of dipole-dipole type. Hypochlorous acid has been postulated as the reactive oxidizing species. The reaction constants involved in the mechanism are derived. The activation parameters are computed with respect to slow step of the mechanism. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0Product Details of 14070-51-0).

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide (cas: 14070-51-0) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Product Details of 14070-51-0

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

Muglu, Halit et al. published their research in Research on Chemical Intermediates in 2020 | CAS: 6590-96-1

2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1) 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.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.Recommanded Product: 6590-96-1

Synthesis, characterization, and antioxidant activity of some new N4-arylsubstituted-5-methoxyisatin-β-thiosemicarbazone derivatives was written by Muglu, Halit. And the article was included in Research on Chemical Intermediates in 2020.Recommanded Product: 6590-96-1 This article mentions the following:

Firstly, thiosemicarbazides were prepared by the reaction of hydrazine monohydrate with isothiocyanates in cold dry ethanol at 0° for 1 h. After that, new isatin-β-thiosemicarbazones I (R = 2-MeC6H4, 4-MeOC6H4, 4-FC6H4, etc.) were synthesized by treatment of 5-methoxyisatin with thiosemicarbazides in aqueous ethanol containing one drop of hydrochloric acid at reflux for 3 h. All the synthesized compounds were evaluated for their antioxidant activity by 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical scavenging method. The synthesized mols. showed lower antioxidant activity than the standard trolox (8.757μM). IC50 values of the newly synthesized isatin-β-thiosemicarbazone derivatives ranged from 12.455 to 73.471μM. In the experiment, the researchers used many compounds, for example, 2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1Recommanded Product: 6590-96-1).

2,4-Dichlorophenylisothiocyanate (cas: 6590-96-1) 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.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.Recommanded Product: 6590-96-1

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

Choi, Bo Seung et al. published their research in Organic Process Research & Development in 2005 | CAS: 96568-04-6

Ethyl 3-(2,6-Dichloro-5-fluoro-3-pyridyl)-3-oxopropionate (cas: 96568-04-6) 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.Category: chlorides-buliding-blocks

Efficient and Scalable Synthesis of Ethyl 2,6-Dichloro-5-Fluoronicotinoyl Acetate Using the Blaise Reaction as a Key Step was written by Choi, Bo Seung;Chang, Jay Hyok;Choi, Hyeong-wook;Kim, Young Keun;Lee, Ki Kon;Lee, Kyu Woong;Lee, Jae Hoon;Heo, Taeho;Nam, Do Hyun;Shin, Hyunik. And the article was included in Organic Process Research & Development in 2005.Category: chlorides-buliding-blocks This article mentions the following:

An efficient synthesis of 2,6-dichloro-5-fluoronicotinoyl acetate (I) has been accomplished in a single step using the Blaise reaction of Et bromoacetate with 3-cyano-2,6-dichloro-5-fluoropyridine. Use of methanesulfonic acid as an in situ activator of zinc removed the induction period of the Blaise reaction to render it safe and viable for a large-scale operation. In the experiment, the researchers used many compounds, for example, Ethyl 3-(2,6-Dichloro-5-fluoro-3-pyridyl)-3-oxopropionate (cas: 96568-04-6Category: chlorides-buliding-blocks).

Ethyl 3-(2,6-Dichloro-5-fluoro-3-pyridyl)-3-oxopropionate (cas: 96568-04-6) 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.Category: chlorides-buliding-blocks

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