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Benzenecarbodithioic acid, 2-methoxy-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108593-01-7

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108593-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108593-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,5,9 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108593-01:
(8*1)+(7*0)+(6*8)+(5*5)+(4*9)+(3*3)+(2*0)+(1*1)=127
127 % 10 = 7
So 108593-01-7 is a valid CAS Registry Number.

108593-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-methoxybenzenecarbodithioate

1.2 Other means of identification

Product number -
Other names 2-methoxy-dithiobenzoic acid methyl ester

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:108593-01-7 SDS

108593-01-7Relevant academic research and scientific papers

Efficient new protocol to synthesize aromatic and heteroaromatic dithioesters

Abrunhosa, Isabelle,Gulea, Mihaela,Masson, Serge

, p. 928 - 934 (2007/10/03)

A very efficient, high yielding procedure to synthesize substituted aromatic and heteroaromatic dithioesters is described. It involves the reaction between (phenylsulfonyl)methyl (hetero)aromatic derivatives and elemental sulfur in basic medium, followed by alkylation.

Carbophilic versus thiophilic attack in the reaction of metallated aromates and heteroaromates with carbon disulfide

Verkruijsse, H. D.,Brandsma, L.

, p. 95 - 98 (2007/10/02)

Copper(I) halides catalyse the formation of carbodithioates RCSSLi in the reaction of aryl- or heteroaryl-lithium reagents with carbon disulfide.Subsequent addition of methyl iodide gives the dithioesters RCSSCH3 in highh yields.Appreciable amounts of the methyl sulfides RSCH3 and tars are obtained when the reaction with CS2 is carried out in the absence of copper(I) salts, especially in the case of more basic organoalkali compounds.

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