Category: 104-86-9

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. HPLC of Formula: 104-86-9.

Kadu, Vikas D.;Patil, Amruta A.;Shendage, Prajakta R. research published ã€?Oxone-Promoted Synthesis of Bis(indolyl)methanes from Arylmethylamines and Indolesã€? the research content is summarized as follows. An environmentally benign synthesis of 3,3′-bis(indolyl)methanes (BIMs) has been developed from arylmethylamines and indoles under aerobic condition in presence of oxone. The formation of BIMs using ethanol as a green reaction medium represents a good practical method for synthesis. The good tolerance was observed towards various functional groups for exploring substrate scope in presence of oxone and the synthesized BIMs afforded in excellent yields up to 94%.

HPLC of Formula: 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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

Chlorinated organic compounds are found in nearly every class of biomolecules. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Formula: C7H8ClN.

Hosseini-Sarvari, Mona;Sheikh, Hossein research published �Reduced graphene oxide-zinc sulfide (RGO-ZnS) nanocomposite: a new photocatalyst for oxidative cyclization of benzylamines to benzazoles under visible-light irradiation� the research content is summarized as follows. A simple route for the preparation of a reduced graphene oxide-zinc sulfide (RGO-ZnS) nanocomposite via one-pot hydrothermal synthesis has been reported. The chem. composition, morphol., and structure of the RGO-ZnS photocatalyst were fully characterized via standard anal. methods, and then, its photocatalytic applications were surveyed through the synthesis of benzazoles. It was found that the photocatalytic properties of pure ZnS were enhanced with the incorporation of RGO. Herein, authors present the RGO-ZnS composite as a new photocatalyst for the synthesis of benzazoles through oxidative cyclization of benzylamines with 1,2-ortho-phenylene disubstituted compounds as a precursor under room temperature, visible light irradiation, and acid/oxidant-free conditions.

104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., Formula: C7H8ClN

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

Chlorinated organic compounds are found in nearly every class of biomolecules. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Application In Synthesis of 104-86-9.

Hu, Huaanzi;Yu, Ting;Cheng, Sidi;Li, Jing;Gan, Chunfang;Luo, Shuang;Zhu, Qiang research published ã€?Palladium-catalyzed tandem Heck/carbonylation/aminocarbonylation en route to chiral heterocyclic α-ketoamidesã€? the research content is summarized as follows. An unprecedented tandem carbonylation/aminocarbonylation triggered by palladium-catalyzed enantioselective Heck-type exocyclopalladation delivering chiral heterocyclic α-ketoamides was developed. The uncommon double CO insertion into the σ-alkylpalladium intermediate takes place selectively under atm. pressure of CO using alkylamine as the nucleophile. Unique structures hybridizing alkyl α-ketoamides with indolin-2-one containing a C3 all-carbon quaternary stereogenic center and 5,7-dihydro-6H-dibenzo[b,d]azepin-6-one containing a thermodynamically stabilized stereogenic biaryl axis were produced in good yields with excellent enantio- and/or diastereoselectivities.

104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., Application In Synthesis of 104-86-9

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

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Application of C7H8ClN.

Hu, Qizhi;Jiang, Shi;Wu, Yue;Xu, Hongzhong;Li, Guoqing;Zhou, Yu;Wang, Jun research published ã€?Ambient-Temperature Reductive Amination of 5-Hydroxymethylfurfural Over Al₂O₃-Supported Carbon-Doped Nickel Catalystã€? the research content is summarized as follows. An efficient catalytic system for the conversion of 5-hydroxymethylfurfural (HMF) into N-containing compounds over low-cost non-noble-metal catalysts is preferable, but it is challenging to reach high conversion and selectivity under mild conditions. Herein, an Al₂O₃-supported carbon-doped Ni catalyst was obtained via the direct pyrolysis-reduction of a mixture of Ni₃(BTC)₂·12H₂O and Al₂O₃, generating stable Ni(0) species due to the presence of carbon residue. A high yield of 96% was observed in the reductive amination of HMF into 5-hydroxymethyl furfurylamine (HMFA) with ammonia and hydrogen at ambient temperature The catalyst was recyclable and could be applied to the ambient-temperature synthesis of HMF-based secondary/tertiary amines and other biomass-derived amines from the carbonyl compounds The significant performance was attributable to the synergistic effect of Ni(0) species and acidic property of the support Al₂O₃, which promoted the selective ammonolysis of the imine intermediate while inhibiting the potential side reaction of over-hydrogenation.

Application of C7H8ClN, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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

Chlorinated organic compounds are found in nearly every class of biomolecules. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Alkyl chlorides, as versatile building blocks in organic chemistry, are used in the preparation of alcohols, thioethers, alkenes, alkynes, esters, and Grignard reagents. Recommanded Product: (4-Chlorophenyl)methanamine.

Hu, Weiyao;Li, Qiyuan;Xu, Dong;Zhai, Guangyao;Zhang, Shinan;Li, Dong;He, Xiaoxiao;Jia, Jinping;Chen, Jiesheng;Li, Xinhao research published ã€?Rapidly and mildly transferring anatase phase of graphene-activated TiO₂ to rutile with elevated Schottky barrier: Facilitating interfacial hot electron injection for Vis-NIR driven photocatalysisã€? the research content is summarized as follows. Visible and even IR (IR) light-initiated hot electrons of graphene (Gr) catalysts are a promising driven power for green, safe, and sustainable H₂O₂ synthesis and organic synthesis without the limitation of bandgap-dominated narrow light absorption to visible light confronted by conventional photocatalyst. However, the life time of photogenerated hot electrons is too short to be efficiently used for various photocatalytic reactions. Here, we proposed a straightforward method to prolong the lifetime of photogenerated hot electrons from graphene by tuning the Schottky barrier at Gr/rutile interface to facilitate the hot electron injection. The rational design of Gr-coated TiO₂ heterojunctions with interface synergy-induced decrease in the formation energy of the rutile phase makes the phase transfer of TiO₂ support proceed smoothly and rapidly via ball milling. The optimized Gr/rutile dyad could provide a H₂O₂ yield of 1.05 mM·g^-1·h^-1 under visible light irradiation (λ â‰?400 nm), which is 30 times of the state-of-the-art noble-metal-free titanium oxide-based photocatalyst, and even achieves a H₂O₂ yield of 0.39 mM·g^-1·h^-1 on photoexcitation by near-IR-region light (âˆ?800 nm).

Recommanded Product: (4-Chlorophenyl)methanamine, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. SDS of cas: 104-86-9.

Hu, Xiao;Tao, Minglin;Ma, Zhongxiao;Zhang, Yi;Li, Yanni;Liang, Deqiang research published ã€?Regioselective Photocatalytic Dialkylation/Cyclization Sequence of 3-Aza-1,5-dienes: Access to 3,4-Dialkylated 4-Pyrrolin-2-onesã€? the research content is summarized as follows. A visible-light-induced regioselective tandem enamido β-C(sp²)-H alkylation/acrylamido alkylation/cyclizative alkenylation sequence of 3-aza-1,5-dienes is presented. This protocol is regiospecific, features a broad substrate scope, and provides a direct access to 3,4-dialkylated 4-pyrrolin-2-ones from readily available N-alkenylacrylamides. It is readily scalable to a gram scale, and could be induced by natural sunlight.

SDS of cas: 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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

Chloride substituents modify the physical properties of organic compounds in several ways. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Related Products of 104-86-9.

Huang, Yan;Shen, Yinjing;Li, Sichen;Zheng, Ruijie;Zhang, Chengjian;Li, Benxia;Zhang, Kun research published ã€?Dual-emission samarium macrocycle as a lab-on-a-molecule enables high-throughput discrimination of anionic sulfonate surfactantsã€? the research content is summarized as follows. Nowadays, it is still a huge challenge to efficiently discriminate of analogus anionic sulfonate surfactants, which are noxious xenobiotics related to many safety concerns of environment and life. Recently, great advances in orthogonal detection have shown the great advantages of principal component anal. (PCA) to construct a comprehensive statistical method for sensing signals in recognizing more analytes with similar structures. Inspired by sensor arrays, we propose a new ′one-element-two-channelâ€?protocol upon a dual-emission samarium macrocycle Sm-2o as the lab-on-a-mol., containing two isolated emissions of macrocycle (443 nm) and Sm(III) (643 nm) emitters as two fluorescence channels. Herein, these targeted surfactants instruct original fluorescences of Sm-2o to generate diverse sensing signals which can finally convert into unique fingerprint patterns and distinguish four anionic surfactants (SDS, SDSO, SCI and AOS) from other ten ones, even their proportional concentrations Significantly, this high-throughput discrimination is realized by different receptor-analyte interactions and the structure transformation of Sm-2o in diverse microenvironments formed in various types of surfactants. Furthermore, these sensing systems also show satisfactory discrimination and semiquantitation performances for mixtures of anionic surfactants, especially the SDS and SDBS, in real water sample, revealing the practicability of our lab-on-a-mol. probe. On the basis of the PCA method, this work provides a vital reference for the design and application of multianalyte chemosensors.

Related Products of 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. COA of Formula: C7H8ClN.

Iakovenko, Roman O.;Chrenko, Daniel;Kristek, Jozef;Desmedt, Eline;Zalesak, Frantisek;De Vleeschouwer, Freija;Pospisil, Jiri research published ã€?Heteroaryl sulfonamide synthesis: Scope and limitationsã€? the research content is summarized as follows. Heteroaryl sulfonamides are important structural motifs in the medicinal and agrochem. industries. However, their synthesis often relies on the use of heteroaryl sulfonyl chlorides, which are unstable and toxic reagents. Herein, the authors report a protocol that allows direct oxidative coupling of heteroaryl thiols R¹SH (R¹ = pyrimidin-2-yl, pyridin-2-yl, 1,3-benzothiazol-2-yl, etc.) to primary amines R²NH₂ (R² = CH₂Ph, CH(Me)CO₂Me, CH(CO₂Me)(CH₂)₂CO₂Me, etc.) and Me (2S)-pyrrolidine-2-carboxylate, readily available and inexpensive commodity chems. The transformation proceeds under mild reaction conditions and yields the desired N-alkylated sulfonamides, e.g., I, in good yields. N-alkyl heteroaryl sulfonamides can be further transformed using a microwave-promoted Fukuyama-Mitsunobu reaction to give N,N-dialkyl heteroaryl sulfonamides. The developed protocols thus enable the preparation of previously difficult to prepare sulfonamides (toxic reagents, harsh conditions, and low yields) under mild conditions.

COA of Formula: C7H8ClN, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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

Organic chlorides are organic molecules with a C-Cl bond, for example chloroform (CH3-Cl) or vinyl chloride(C2H3Cl). 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. Organic chlorides can be used in production of: PVC, Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. Recommanded Product: (4-Chlorophenyl)methanamine.

He, Ben;Zhang, Sikun;Zhang, Yueyan;Li, Guoping;Zhang, Bingjie;Ma, Wenqiang;Rao, Bin;Song, Ruitong;Zhang, Lei;Zhang, Yanfeng;He, Gang research published 《 ortho-Terphenylene Viologens with Through-Space Conjugation for Enhanced Photocatalytic Oxidative Coupling and Hydrogen Evolution》, the research content is summarized as follows. A series of novel ortho-terphenylene viologen derivatives (o-TPV²⁺) with through-space conjugation (TSC) via the combination of ortho-terphenylene skeletons with viologen structure is reported. Their optoelectronic properties can be adjusted by N-arylation or N-alkylation reactions. Compared with other viologen derivatives, o-TPV²⁺ not only exhibits strong photoluminescence, but also retards the charge recombination process and stabilizes diradicals state without forming a quinoid structure due to the special TSC effect. Based on their special redox characteristics, o-TPV²⁺ were applied to the photocatalytic oxidative coupling of benzylamine with 96% yield. In addition, pTA-o-TPV²⁺ (tethered with p-toluic acid) modified g-C₃N₄ was used for visible-light-driven hydrogen production for the first time, exceeding 15 times the rate over unmodified g-C₃N₄.

Recommanded Product: (4-Chlorophenyl)methanamine, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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

Chloride substituents modify the physical properties of organic compounds in several ways. 104-86-9, formula is C7H8ClN, Name is (4-Chlorophenyl)methanamine. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Synthetic Route of 104-86-9.

He, Haiping;Duan, Dehao;Li, Hong;Wei, Yifei;Nie, Liang;Tang, Bo;Wang, Hanyu;Han, Xiaowei;Huang, Panpan;Peng, Xiangjun research published 《 Graphene oxide-catalyzed synthesis of benzothiazoles with amines and elemental sulfur via oxidative coupling strategy of amines to imines》, the research content is summarized as follows. The graphene oxide-catalyzed coupling and cyclization reactions of primary amines with elemental sulfur was developed to afford optically property benzothiazoles I [R = Ph, 4-MeC₆H₄, 2-F₃C₆H₄, etc.], II [R¹ = H, 3-CF₃, 4-Me, etc.] and III [R¹ = H, 2-CF₃, 4-Cl, etc.; R² = H, 6-Cl, 6-OMe, etc.]. This coupling and cyclization strategies proceeded under the oxidant system graphene oxide/O₂ and constructed carbon-heteroatom (N, S) bonds with amines and elemental sulfur. Due to benzothiazoles as common chromophores, these products exhibited intriguing fluorescence properties, including outstanding Stokes shifts (up to 161 nm) and quantum yields (up to 74%). Utilizing the products’ unique fluorescence response in different solvents, β-naphthothiazole II [R¹ = H] showed excellent aggregation-induced emission properties in 1,2-dichloroethane, which was 60 times higher than in THF.

Synthetic Route of 104-86-9, 4-Chlorobenzylamine is a useful research compound. Its molecular formula is C7H8ClN and its molecular weight is 141.6 g/mol. The purity is usually 95%.
4-Chlorobenzylamine is a reactant in the environmentally friendly synthesis of pyrroles.
4-Chlorobenzylamine is a chemical that is used as an intermediate in the synthesis of other compounds. It has low bioavailability, which may be due to its reactive site. The chemical can be characterized using nmr spectra and potent inhibitory activity. 4-Chlorobenzylamine has been found to react with nitrogen atoms, and this reaction is highly acidic. FT-IR spectroscopy can also be used to characterize this compound. Intermolecular hydrogen bonding and hydroxyl group are two of the major interactions of 4-chlorobenzylamine with other molecules. This chemical reacts with serine protease, glyoxal, and other substances in a manner that depends on the molecule’s structure., 104-86-9.

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