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Benzene, 1-chloro-3-[(phenylthio)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51229-52-8

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51229-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51229-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,2 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51229-52:
(7*5)+(6*1)+(5*2)+(4*2)+(3*9)+(2*5)+(1*2)=98
98 % 10 = 8
So 51229-52-8 is a valid CAS Registry Number.

51229-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chlorobenzyl phenyl sulfide

1.2 Other means of identification

Product number -
Other names (3-Chlor-benzyl)-phenyl-sulfid

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:51229-52-8 SDS

51229-52-8Relevant academic research and scientific papers

Alkyl Sulfides as Promising Sulfur Sources: Metal-Free Synthesis of Aryl Alkyl Sulfides and Dialkyl Sulfides by Transalkylation of Simple Sulfides with Alkyl Halides

Liu, Ting,Qiu, Renhua,Zhu, Longzhi,Yin, Shuang-Feng,Au, Chak-Tong,Kambe, Nobuaki

supporting information, p. 3833 - 3837 (2018/12/05)

A site-selective metal-free dealkylative approach to synthesize aryl alkyl and symmetrical dialkyl sulfides has been developed. This procedure is convenient and has wide functional group tolerance giving rise to sulfides carrying various alkyl chains from simple alkyl sulfides and alkyl halides in good to excellent yields. This transalkylation proceeds by an ionic mechanism via sulfonium intermediates and it was proposed that dimethylacetamide (DMAC) may participate in part to promote the reaction.

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