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175464-51-4

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175464-51-4 Usage

General Description

3-(ChloroMethyl)benzylalcohol is a chemical compound with the formula C8H9ClO. It is a colorless liquid with a mild, pleasant odor and is used as a reagent in organic synthesis. 3-(ChloroMethyl)benzylalcohol is commonly used as a raw material in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also employed as an intermediate in the manufacturing of various substances, such as dyes, surfactants, and perfumes. Additionally, 3-(ChloroMethyl)benzylalcohol has antimicrobial properties and is utilized as a preservative in personal care products and industrial applications. Overall, this chemical is an important building block in the synthesis of various organic compounds and finds widespread use in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 175464-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,6 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 175464-51:
(8*1)+(7*7)+(6*5)+(5*4)+(4*6)+(3*4)+(2*5)+(1*1)=154
154 % 10 = 4
So 175464-51-4 is a valid CAS Registry Number.

175464-51-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(chloromethyl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names m-hydroxymethylbenzyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:175464-51-4 SDS

175464-51-4Relevant articles and documents

Novel unsymmetrical PCP′ pincer ligands and their palladium(II) complexes

Eberhard, Michael R.,Matsukawa, Shiro,Yamamoto, Yohsuke,Jensen, Craig M.

, p. 185 - 189 (2003)

Synthetic routes towards novel PCP′ pincer ligands were devised. Ligand 1-(Pr2iPOCH2) -3-(Bu2tPCH2) (C6H4) is prepared in a three step synthesis from 1,3-benzenedimethanol and 1-(Pr2iPO)-3- (Bu2tPCH2)(C6H4) is accessible in three steps from 3-hydroxybenzylalcohol. Both their palladium(II) complexes are prepared in good yields but are distinctly different since [PdCl{(C6H3) (OPPr2i)-2-(CH2PBu2 t)-6}] possesses two five-membered palladacycles, whereas [PdCl{(C6H3)(CH2PBu2 t)-2-(CH2OPPr2i)-6}] is unusual for a pincer complex in that it contains both five- and six-membered palladacycles. Both compounds also represent the first examples of pincer complexes where one donor is a phosphinite and the other is a phosphine. The X-ray structures of these complexes were solved and are discussed. The data reveal that an increase in the metallacycle ring-size leads to changes in bond lengths, but more importantly to significant increases in the bond angles.

Highly chemo- and regio-selective hydroxylations of o- and m-substituted toluenes to benzyl alcohols with Cellulosimicrobium cellulans EB-8-4

Dai, Shiyao,Wu, Jinchuan,Wang, Zunsheng,Chen, Yongzheng,Li, Zhi

experimental part, p. 6919 - 6923 (2010/09/18)

Highly chemo- and regio-selective benzylic hydroxylations of o- and m-substituted toluenes were achieved with the easily available and easy-to-handle resting cells of Cellulosimicrobium cellulans EB-8-4 as biocatalysts, giving the corresponding benzyl alcohols as single product. Benzyl alcohols were obtained in 78-94% yield, demonstrating the first green, clean, and simple method for the preparation of benzyl alcohols via hydroxylations. Biotransformation of 4-methylbenzyl chloride with the same strain gave 4-methylbenzyl alcohol in 67-81% yield, suggesting a novel dehalogenation activity of the cells and providing a novel, green, and efficient method for the preparation of 4-methylbenzyl alcohol as well as the application potential in biodegradation of chlorine-containing aromatics.

Synthesis and resolution of planar-chiral ruthenium-palladium complexes with ECE' pincer ligands

Bonnet, Sylvestre,Li, Jie,Siegler, Maxime A.,Von Chrzanowski, Lars S.,Spek, Anthony L.,Van Koten, Gerard,Klein Gebbink, Robertus J. M.

supporting information; scheme or table, p. 3340 - 3343 (2009/12/27)

The synthesis and chiral resolution of the first planar-chiral ECE'-metal complexes of type e was reported. n1-coordination of the metal (M) was carried out first, followed by n6 of a second metal fragment (M'). The ECE'-palladium co

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