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4-Methoxydithiobenzoic acid ethyl ester is an organic compound with the chemical formula C10H10O2S2. It is a colorless to pale yellow liquid with a molecular weight of 226.31 g/mol. 4-Methoxydithiobenzoic acid ethyl ester is characterized by the presence of a benzene ring with a methoxy group at the 4-position, two sulfur atoms attached to the benzene ring through single bonds, and an ethyl ester group. It is used as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. The compound is known for its reactivity and can participate in various chemical reactions, such as nucleophilic substitutions and redox processes. Due to its specific functional groups, it is also used in the preparation of dyes and pigments.

942-85-8

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942-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 942-85-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 942-85:
(5*9)+(4*4)+(3*2)+(2*8)+(1*5)=88
88 % 10 = 8
So 942-85-8 is a valid CAS Registry Number.

942-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-methoxybenzenecarbodithioate

1.2 Other means of identification

Product number -
Other names 4-Methoxy-dithiobenzoesaeure-aethylester

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:942-85-8 SDS

942-85-8Relevant academic research and scientific papers

New Synthesis and Some Reactions of Vinyl Arenecarbodithioates. Wittig Reaction of (Triphenylphosphonio)methyl Arenecarbodithioate Iodides

Ishida, Masaru,Kaga, Koh-ichi,Sato, Hiroyuki,Yokoi, Masato,Kato, Shinzi

, p. 1403 - 1410 (2007/10/02)

Wittig reaction of new phosphonium salts, (triphenylphosphonio)methyl arenecarbodithioate iodides, with variety of aldehydes gave the corresponding vinyl dithiocarboxylate with nucleophiles such as potassium alkoxide or alkanethiolate was investigated and found to give the thioacylated products in high yields.Ab initio molecular orbital calculations of the model compound vinyl dithioformate, are also discussed.

Raney Nickel Desulphuration of Some Dithioacid Derivatives

Latif, K. A.,Ali, M. Umar

, p. 471 - 473 (2007/10/02)

Raney Nickel desulphuration of some bisthioaroyl disulphides (I), and lead salts (II) and esters (III) of dithioacids with W-2A, W-2B and W-2C catalysts has been investigated.In some cases dimorphic products are obtained.

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