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83818-62-6

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83818-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83818-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,1 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83818-62:
(7*8)+(6*3)+(5*8)+(4*1)+(3*8)+(2*6)+(1*2)=156
156 % 10 = 6
So 83818-62-6 is a valid CAS Registry Number.

83818-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-1-(phenylthio)-1-octene

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:83818-62-6 SDS

83818-62-6Relevant articles and documents

REGIOSPECIFIC HYDROGEN CHLORIDE ELIMINATION FROM α,β-DICHLOROALKYL PHENYL SULPHIDES

Bellesia, Franco,Ghelfi, Franco,Pagnoni, Ugo Maria,Pinetti, Adriano

, p. 337 - 340 (2007/10/02)

α,β-Dichloroalkyl phenyl sulphides undergo regiospecific hydrogen chloride eliminations to afford α- or β-chloro-1-alkenyl phenyl sulphides in good yields.

Synthesis of Carboxylic Acids and their Methyl Esters from Alkyl Phenyl Sulfides

Fortes, Carlos C.,Fortes, Helena C.,Goncalves, Dioneia C. R. G.

, p. 857 - 858 (2007/10/02)

Alkl phenyl sulfides are converted with sulphuryl chloride and pyridine under controlled temperatures into 1,1-dichloroalkyl phenyl sulfides or 1-chloro-1-enyl sulfides; treatment of these intermediates with methanol-water (1percent v/v) and mercury(II) acetate-formic acid gives, respectively, methyl carboxylic ester and carboxylic acids.

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