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4-Methoxy-benzenecarbothioic acid methyl ester, also known as methyl 4-methoxybenzenecarbothioate, is an organic compound with the chemical formula C9H10OS2. It is a colorless to pale yellow liquid that is soluble in organic solvents. 4-METHOXY-BENZENECARBODITHIOIC ACID METHYL ESTER is characterized by the presence of a 4-methoxy group attached to a benzene ring, with a dithiocarboxylate group and a methyl ester functional group. It is used as an intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its reactivity, it is important to handle this chemical with care, following appropriate safety measures to prevent potential health and environmental risks.

5874-09-9

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5874-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5874-09-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5874-09:
(6*5)+(5*8)+(4*7)+(3*4)+(2*0)+(1*9)=119
119 % 10 = 9
So 5874-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10OS2/c1-10-8-5-3-7(4-6-8)9(11)12-2/h3-6H,1-2H3

5874-09-9SDS

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 4-METHOXY-BENZENECARBODITHIOIC ACID METHYL ESTER

1.2 Other means of identification

Product number -
Other names 4-Methoxy-benzenecarbodithioic 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 -
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More Details:5874-09-9 SDS

5874-09-9Relevant academic research and scientific papers

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.

Aromatic Substitution. 46. Methyl (Ethyl) Thio(Dithio)carboxylation of Aromatics with S-Methyl (S-Ethyl) Thiocarboxonium and Dithiocarboxonium Fluoroantimonates

Olah, George A.,Bruce, Mark R.,Clouet, Francoise L.

, p. 438 - 442 (2007/10/02)

S-Methyl(S-ethyl)thio(dithio)carboxinium ions were prepared by reacting methyl(ethyl) fluoride-antimony pentafluoride with carbonyl sulfide (carbon disulfide) and studied with 1H and 13C NMR spectroscopy.The ions were subsequently used in the novel carboxylation reaction of arenes to S-methyl (S-ethyl) thio(dithio)benzoates.The method was also found to be adaptable to the carboxylation of polystyrene to poly(styrenecarboxylic acid) without degradation of the polymer backbone.

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