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Benzene, 1-[(2-chloro-2-propenyl)thio]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53299-60-8

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53299-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53299-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,9 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53299-60:
(7*5)+(6*3)+(5*2)+(4*9)+(3*9)+(2*6)+(1*0)=138
138 % 10 = 8
So 53299-60-8 is a valid CAS Registry Number.

53299-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloroprop-2-enylsulfanyl)-4-methylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-[(2-chloro-2-propenyl)thio]-4-methyl

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:53299-60-8 SDS

53299-60-8Relevant academic research and scientific papers

INTERMEDIATES TO PREPARE PYRIDAZINONE HERBICIDES, AND A PROCESS TO PREPARE THEM

-

Paragraph 0086; 0087; 0088, (2018/02/10)

Disclosed is a process for preparing a compound of Formula1,from a compound of Formula2wherein X, R 1 , R 2 , R 3 , R 4 , R 5 , n, R 6 , R 7 , G and W are as defined in the disclosure. Also disclosed are compounds of Formulae2and4wherein X, R 1 , R 2 , R

Highly chemoselective synthesis of aryl allylic sulfoxides through calcium hypobromite oxidation of aryl allylic sulfides

Pace, Vittorio,Castoldi, Laura,Holzer, Wolfgang

supporting information; experimental part, p. 967 - 972 (2012/03/11)

A highly chemoselective oxidation of widely substituted aryl allylic sulfides, prepared by allylation of arylthioethers with KF-Celite, to the corresponding aryl allylic sulfoxide was achieved by employing calcium hypobromite. Neither over-oxidation to sulfones nor halogenation of the aromatic rings was observed. The protocol may be successfully applied for the oxidation of substituted allylic systems (i.e., 2-haloallyl) that per se could interact with the oxidizing agent.

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