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Welcome to talk about 95-49-8, If you have any questions, you can contact McGuire, RT; Yadav, AA; Stradiotto, M or send Email.. Product Details of 95-49-8

Product Details of 95-49-8. McGuire, RT; Yadav, AA; Stradiotto, M in [McGuire, Ryan T.; Stradiotto, Mark] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4R2, Canada; [Yadav, Arun A.] Paraza Pharma Inc, 2525 Ave Marie Curie, Montreal, PQ H4S 2E1, Canada published Nickel-Catalyzed N-Arylation of Fluoroalkylamines in 2021.0, Cited 51.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

The Ni-catalyzed N-arylation of beta-fluoroalkylamines with broad scope is reported for the first time. Use of the air-stable pre-catalyst (PAd2-DalPhos)Ni(o-tol)Cl allows for reactions to be conducted at room temperature (25 degrees C, NaOtBu), or by use of a commercially available dual-base system (100 degrees C, DBU/NaOTf), to circumvent decomposition of the N-(beta-fluoroalkyl)aniline product. The mild protocols disclosed herein feature broad (hetero)aryl (pseudo)halide scope (X=Cl, Br, I, and for the first time phenol-derived electrophiles), encompassing base-sensitive substrates and enantioretentive transformations, in a manner that is unmatched by any previously reported catalyst system.

Welcome to talk about 95-49-8, If you have any questions, you can contact McGuire, RT; Yadav, AA; Stradiotto, M or send Email.. Product Details of 95-49-8

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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Welcome to talk about 87-63-8, If you have any questions, you can contact Du, GY; Rao, SM; Gurbani, D; Henning, NJ; Jiang, J; Che, JW; Yang, A; Ficarro, SB; Marto, JA; Aguirre, AJ; Sorger, PK; Westover, KD; Zhang, TH; Gray, NS or send Email.. Recommanded Product: 2-Chloro-6-methylaniline

Recommanded Product: 2-Chloro-6-methylaniline. In 2020 J MED CHEM published article about CELL LUNG-CANCER; IRREVERSIBLE INHIBITORS; FAMILY KINASES; DISCOVERY; GROWTH; RESISTANCE; PROTEIN; OPTIMIZATION; ACTIVATION; EXPRESSION in [Gurbani, Deepak; Westover, Kenneth D.; Zhang, Tinghu] Univ Texas Southwestern Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA; [Gurbani, Deepak; Westover, Kenneth D.; Zhang, Tinghu] Univ Texas Southwestern Med Ctr Dallas, Dept Radiat Oncol, Dallas, TX 75390 USA; [Du, Guangyan; Rao, Suman; Henning, Nathaniel J.; Jiang, Jie; Che, Jianwei; Ficarro, Scott B.; Marto, Jarrod A.; Westover, Kenneth D.; Zhang, Tinghu; Gray, Nathanael S.] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA; [Du, Guangyan; Rao, Suman; Henning, Nathaniel J.; Jiang, Jie; Che, Jianwei; Westover, Kenneth D.; Zhang, Tinghu; Gray, Nathanael S.] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02215 USA; [Yang, Annan; Aguirre, Andrew J.] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA; [Sorger, Peter K.] Harvard Med Sch, Lab Syst Biol, Boston, MA 02115 USA in 2020, Cited 51. The Name is 2-Chloro-6-methylaniline. Through research, I have a further understanding and discovery of 87-63-8.

SRC is a major regulator of many signaling pathways and contributes to cancer development. However, development of a selective SRC inhibitor has been challenging, and FDA-approved SRC inhibitors, dasatinib and bosutinib, are multitargeted kinase inhibitors. Here, we describe our efforts to develop a selective SRC covalent inhibitor by targeting cysteine 277 on the P-loop of SRC. Using a promiscuous covalent kinase inhibitor (CKI) SM1-71 as a starting point, we developed covalent inhibitor 15a, which discriminates SRC from other covalent targets of SM1-71 including TAK1 and FGFR1. As an irreversible covalent inhibitor, compound 15a exhibited sustained inhibition of SRC signaling both in vitro and in vivo. Moreover, 15a exhibited potent antiproliferative effects in nonsmall cell lung cancer cell lines harboring SRC activation, thus providing evidence that this approach may be promising for further drug development efforts.

Welcome to talk about 87-63-8, If you have any questions, you can contact Du, GY; Rao, SM; Gurbani, D; Henning, NJ; Jiang, J; Che, JW; Yang, A; Ficarro, SB; Marto, JA; Aguirre, AJ; Sorger, PK; Westover, KD; Zhang, TH; Gray, NS or send Email.. Recommanded Product: 2-Chloro-6-methylaniline

Reference:
Patent; ASTRAZENECA AB; NPS PHARMACEUTICALS, INC.; WO2006/20879; (2006); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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Welcome to talk about 95-49-8, If you have any questions, you can contact Rendon-Nava, D; Alvarez-Hernandez, A; Rheingold, AL; Suarez-Castillo, OR; Mendoza-Espinosa, D or send Email.. HPLC of Formula: C7H7Cl

An article Hydroxyl-functionalized triazolylidene-based PEPPSI complexes: metallacycle formation effect on the Suzuki coupling reaction WOS:000460302800037 published article about PD-NHC PRECATALYST; HETEROCYCLIC CARBENE COMPLEXES; ORTHO-SUBSTITUTED BIARYLS; PALLADIUM COMPLEXES; ARYL CHLORIDES; C-N; ROOM-TEMPERATURE; HIGHLY EFFICIENT; LIGANDS SYNTHESIS; MIYAURA in [Rendon-Nava, David; Alvarez-Hernandez, Alejandro; Suarez-Castillo, Oscar R.; Mendoza-Espinosa, Daniel] Univ Autonoma Estado Hidalgo, Area Acad Quim, Carretera Pachuca Tulancingo Km 4-5, Mineral De La Reforma 42090, Hidalgo, Mexico; [Rheingold, Arnold L.] Univ Calif San Diego, Dept Chem & Biochem, 9500 Gilman Dr, La Jolla, CA 92093 USA in 2019, Cited 100. HPLC of Formula: C7H7Cl. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8

We report the preparation and full characterization of a series of hydroxyl functionalized 1,2,3-triazolylidene- based PEPPSI complexes 2a-c and their catalytic application in the Suzuki cross coupling reaction of aryl chlorides/ amides with boronic acids. Under basic reaction conditions, complexes 2a-c show a notable increase in their catalytic efficiency compared with two ether-wingtip functionalized PEPPSI analogues (3 and 4) and a commercially available NHC-Pd complex (5). The catalytic results suggest that deprotonation of the hydroxyl group in complexes 2a-c plays an important role in the overall process. Deprotonation of the alcohol moiety of complexes 2a-b with sodium tert-butoxide allows for the isolation of metallacycles 6a-b, which are proposed as the active species of cross coupling reactions.

Welcome to talk about 95-49-8, If you have any questions, you can contact Rendon-Nava, D; Alvarez-Hernandez, A; Rheingold, AL; Suarez-Castillo, OR; Mendoza-Espinosa, D or send Email.. HPLC of Formula: C7H7Cl

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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Authors Zhu, XJ; Liu, Y; Liu, C; Yang, HJ; Fu, H in ROYAL SOC CHEMISTRY published article about PHOTOREDOX CATALYSIS; CARBOXYLIC-ACIDS; TRIFLUOROMETHYLATION; ACTIVATION; ALCOHOLS; ALKYLATION; ALDEHYDES; CLEAVAGE; ESTERS in [Zhu, Xianjin; Liu, Yong; Liu, Can; Yang, Haijun; Fu, Hua] Tsinghua Univ, Dept Chem, Minist Educ, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China in 2020, Cited 59. HPLC of Formula: C7H7Cl. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8

Visible light-induced organic reactions are important chemical transformations in organic chemistry, and their efficiency highly depends on suitable photocatalysts. However, the commonly used photocatalysts are precious transition-metal complexes and elaborate organic dyes, which hamper large-scale production due to high cost. Here, for the first time, we report a novel strategy: light and oxygen-enabled sodium trifluoromethanesulfinate-mediated selective oxidation of C-H bonds, allowing high-value-added aromatic ketones and carboxylic acids to be easily prepared in high-to-excellent yields using readily available alkyl arenes, methyl arenes and aldehydes as materials. The mechanistic investigations showed that the treatment of inexpensive and readily available sodium trifluoromethanesulfinate with oxygen under irradiation of light couldin situform a pentacoordinate sulfide intermediate as an efficient photosensitizer. The method represents a highly efficient, economical and environmentally friendly strategy, and the light and oxygen-enabled sodium trifluoromethanesulfinate photocatalytic system represents a breakthrough in photochemistry.

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Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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SDS of cas: 95-49-8. Welcome to talk about 95-49-8, If you have any questions, you can contact Mohammadpour, P; Safaei, E or send Email.

SDS of cas: 95-49-8. I found the field of Chemistry very interesting. Saw the article Catalytic C-H aerobic and oxidant-induced oxidation of alkylbenzenes (including toluene derivatives) over VO2+ immobilized on core-shell Fe3O4@SiO2 at room temperature in water published in 2020.0, Reprint Addresses Safaei, E (corresponding author), Shiraz Univ, Coll Sci, Dept Chem, Shiraz 7194684795, Iran.. The CAS is 95-49-8. Through research, I have a further understanding and discovery of 1-Chloro-2-methylbenzene.

Direct C-H bond oxidation of organic materials, and producing the necessary oxygenated compounds under mild conditions, has attracted increasing interest. The selective oxidation of various alkylbenzenes was carried out by means of a new catalyst containing VO2+ species supported on silica-coated Fe3O4 nanoparticles usingt-butyl hydroperoxide as an oxidant at room temperature in H2O or solvent-free media. The chemical and structural characterization of the catalyst using several methods such as FTIR spectroscopy, XRD, FETEM, FESEM, SAED, EDX and XPS showed that VO2+ is covalently bonded to the silica surface. High selectivity and excellent conversion of various toluene derivatives, with less reactive aliphatic (sp(3)) C-H bonds, to related benzoic acids were quite noticeable. The aerobic oxygenation reaction of these alkylbenzenes was studied under the same conditions. All the results accompanied by sustainability of the inexpensive and simple magnetically separable heterogeneous catalyst proved the important criteria for commercial applications.

SDS of cas: 95-49-8. Welcome to talk about 95-49-8, If you have any questions, you can contact Mohammadpour, P; Safaei, E or send Email.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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About 2-Chloro-6-methylaniline, If you have any questions, you can contact Colomer, I or concate me.. COA of Formula: C7H8ClN

COA of Formula: C7H8ClN. In 2020 ACS CATAL published article about HYDROGEN-EXCHANGE; AROMATIC-AMINES; SUBSTITUTED DIALKYLANILINES; ALKYLATION; ACTIVATION; MECHANISM; ACID in [Colomer, Ignacio] Univ Autonoma Madrid, Dept Organ Chem, Madrid 28049, Spain; [Colomer, Ignacio] IMDEA Nanociencia, Madrid 28049, Spain in 2020, Cited 65. The Name is 2-Chloro-6-methylaniline. Through research, I have a further understanding and discovery of 87-63-8.

Providing new methods for the selective functionalization of small molecules is highly desirable, because installing molecular diversity in a desired position, for example, allows one to modulate bioactive molecules. This work reports a method for the selective functionalization of anilines using hexafluoroisopropanol (HFIP) as a solvent to promote an acid-catalyzed hydroarylation of olefins. Mechanistic experiments revealed that HFIP both protonates the alkene and selectively enables anilines toward the electrophilic aromatic substitution. This powerful strategy has been applied to the functionalization of the anti-inflammatory mefenamic acid with chemocontrol and regiocontrol.

About 2-Chloro-6-methylaniline, If you have any questions, you can contact Colomer, I or concate me.. COA of Formula: C7H8ClN

Reference:
Patent; ASTRAZENECA AB; NPS PHARMACEUTICALS, INC.; WO2006/20879; (2006); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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In 2020.0 ADV SYNTH CATAL published article about N-HETEROCYCLIC CARBENE; DIRECT C-5 ARYLATION; HIGHLY EFFICIENT; DIRECT (HETERO)ARYLATION; DIRECT C5-ARYLATION; METAL-COMPLEXES; HECK REACTION; IMIDAZOLES; BOND; FUNCTIONALIZATION in [Lee, Jhen-Yi; Ghosh, Debalina; Kuo, Ya-Ting; Lee, Hon Man] Natl Changhua Univ Educ, Dept Chem, Changhua 50058, Taiwan in 2020.0, Cited 85.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Product Details of 95-49-8

A series of dimetallic palladium(II)-NHC complexes comprised of 1,4-naphthalenyl or 9,10-anthracenyl spacer sandwiched between two imidazole rings was successfully synthesized. These complexes were characterized by H-1 and C-13{H-1} NMR spectroscopy and elemental analysis. The structures of two dimetallic palladium complexes and a related mononuclear palladium complex to be used for comparative studies were further characterized by X-ray diffraction. The dimetallic palladium complex with the 9,10-anthracenyl linker was very efficient in catalyzing direct C-H arylation reactions of heteroaromatic compounds (imidazoles, imidazo[1,2-a]pyridine, and thioazole) with a broad range of aryl chlorides, employing a mild monopalladium loading of 1.5 mol%. It allows for the effective use of aryl chlorides to prepare arylated heterocycles, previously only accessible with the more reactive bromide counterparts. Importantly, the catalytic activity of the dimetallic precatalyst was found to be higher than that of an analogous mononuclear complex.

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Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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Category: chlorides-buliding-blocks. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Das, S; Murugesan, K; Rodriguez, GJV; Kaur, J; Barham, JP; Savateev, A; Antonietti, M; Konig, B or concate me.

An article Photocatalytic (Het)arylation of C(sp(3))-H Bonds with Carbon Nitride WOS:000618540300047 published article about C-H BONDS; LIGHT PHOTOREDOX CATALYSIS; HYDROGEN-PRODUCTION; FUNCTIONALIZATION; ARYLATION; PHOTOCHEMISTRY; ALKYLATION; CO2 in [Das, Saikat; Murugesan, Kathiravan; Rodriguez, Gonzalo J. Villegas; Kaur, Jaspreet; Barham, Joshua P.; Koenig, Burkhard] Univ Regensburg, Fak Chem & Pharm, D-93040 Regensburg, Germany; [Savateev, Aleksandr; Antonietti, Markus] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14424 Potsdam, Germany in 2021.0, Cited 74.0. Category: chlorides-buliding-blocks. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8

Graphitic carbon nitride materials have attracted significant interest in recent years and found applications in diverse light-to-energy conversions such as artificial photosynthesis, CO2 reduction, or degradation of organic pollutants. However, their utilization in synthetic photocatalysis, especially in the direct functionalization of C(sp(3))-H bonds, remains underexplored. Herein, we report mesoporous graphitic carbon nitride (mpg-CN as a heterogeneous organic semiconductor photocatalyst for direct arylation of C(sp(3))-H bonds in combination with nickel catalysis. Our protocol has a broad synthetic scope (>70 examples including late-stage functionalization of drugs and agrochemicals), is operationally simple, and shows high chemo- and regioselectivities. Facile separation and recycling of the mpg-CN catalyst in combination with its low preparation cost, innate photochemical stability, and low toxicity are beneficial features overcoming typical shortcomings of homogeneous photocatalysis. Detailed mechanistic investigations and kinetic studies indicate that an unprecedented energy-transfer process (EnT) from the organic semiconductor to the nickel complex is operating.

Category: chlorides-buliding-blocks. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Das, S; Murugesan, K; Rodriguez, GJV; Kaur, J; Barham, JP; Savateev, A; Antonietti, M; Konig, B or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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Safety of 1-Chloro-2-methylbenzene. Muzzio, M; Lin, HH; Wei, KC; Guo, XF; Yu, C; Yom, T; Xi, Z; Yin, ZY; Sun, SH in [Muzzio, Michelle; Lin, Honghong; Wei, Kecheng; Guo, Xuefeng; Yu, Chao; Yom, Typher; Yin, Zhouyang; Sun, Shouheng] Brown Univ, Dept Chem, Providence, RI 02912 USA; [Xi, Zheng] Univ Cent Florida, Dept Chem, Orlando, FL 32816 USA published Efficient Hydrogen Generation from Ammonia Borane and Tandem Hydrogenation or Hydrodehalogenation over AuPd Nanoparticles in 2020.0, Cited 50.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

Alternatives to the use of pressurized hydrogen (H-2) in chemical syntheses are of growing interest and importance in developing safer protocols. Ammonia borane (AB), with its high hydrogen content and ability to release H-2 under mild conditions, is one potential solution. However, optimization of AB dehydrogenation and further the use of AB as a H-2 source to facilitate tandem one-pot reactions with both high activity and stability is an ongoing research challenge. In this work, monodisperse AuPd nanoparticle (NP) catalysts were synthesized and systematically studied for AB dehydrogenation, and Au-rich NPs were found to be the most active composition for AB methanolysis with a turnover frequency (TOF) of 160 min(-1) surpassing most Pd-based NP catalysts to date. More importantly, Au-rich NPs were also active in the one-pot tandem reduction of a series of nitro-groups and the hydrodehalogenation of mono- and polyhalogenated persistent chemical pollutants under mild reaction conditions using only a 2:1 molar ratio of AB to substrate. The AuPd catalyst was stable after ten reaction runs for AB methanolysis and five reaction runs for tandem one-pot reactions without a loss of activity or change in NP structure and morphology.

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Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

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COA of Formula: C7H7Cl. Welcome to talk about 95-49-8, If you have any questions, you can contact Nakajima, M; Miyamoto, K; Hirano, K; Uchiyama, M or send Email.

An article Diaryl-lambda(3)-chloranes: Versatile Synthesis and Unique Reactivity as Aryl Cation Equivalent WOS:000466053400013 published article about STEREOSELECTIVE-SYNTHESIS; DIARYLIODONIUM SALTS; ALPHA-PHENYLATION; FLUORONIUM ION; ANIONS; (Z)-ENETHIOLS; GENERATION; ARYLATION; RESONANCE; BROMONIUM in [Nakajima, Misuzu; Miyamoto, Kazunori; Hirano, Keiichi; Uchiyama, Masanobu] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan; [Uchiyama, Masanobu] RIKEN, Adv Elements Chem Lab, CPR, 2-1 Hirosawa, Wako, Saitama 3510198, Japan; [Uchiyama, Masanobu] Shinshu Univ, RISM, Ueda, Nagano 3868567, Japan in 2019.0, Cited 53.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. COA of Formula: C7H7Cl

We have developed a versatile, high-yield synthesis of diarylchloroniums/lambda(3)-chloranes through the reaction of various chloroarenes with readily prepared mesityldiazonium tetrakis(pentafluorophenyl)borate under mild conditions. The scope of the reaction is broad, including ArCl, ArBr, and ArI. The diarylchloroniums/lambda(3)-chloranes prepared here show unique reactivity in various respects, enabling intermolecular electrophilic arylation reaction of weak nucleophiles, and chlorane-halogane exchange reaction.

COA of Formula: C7H7Cl. Welcome to talk about 95-49-8, If you have any questions, you can contact Nakajima, M; Miyamoto, K; Hirano, K; Uchiyama, M or send Email.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics