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

67207-64-1

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67207-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67207-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,0 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67207-64:
(7*6)+(6*7)+(5*2)+(4*0)+(3*7)+(2*6)+(1*4)=131
131 % 10 = 1
So 67207-64-1 is a valid CAS Registry Number.

67207-64-1SDS

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 2-methoxy-2-methyl-1-propyl 4-chlorophenyl sulfide

1.2 Other means of identification

Product number -
Other names -

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:67207-64-1 SDS

67207-64-1Downstream Products

67207-64-1Relevant academic research and scientific papers

The products of the reaction of thiiranium ions with competing nucleophiles

Schmid, George H.,Strukelj, Mark,Dalipi, Snezana

, p. 1945 - 1950 (2007/10/02)

The reaction of the stable thiiranium ion, prepared by the reaction of trilfuoromethanesulfonic acid and methyl-3-(4-chlorophenylthio)propene with tetraethylammonium chloride in either 3.5 or 36percent v/v methanol/dichloromethane with urea as a buffer, forms 2-methoxy-2-methyl-1-propyl 4-chlorophenyl sulfide, 2-chloro-2-methyl-1-propyl 4-chlorophenyl sulfide, and 1-chloro-2-methyl-2-propyl 4-chlorophenyl sulfide as products.While these same products are formed by the addition of 4-chlorobenzenesulfenyl chloride to methylpropene in the same solvents, their proportions differ.This is one of the rare examples in which there is a difference in the product compositon of thiiranium ions formed in different ways and alloowed to react under identical conditions.One possible explanation for this difference may be that the two thiiranium ions form products by different kinds of ion pairs.

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