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Dithiocarbonic acid O-methyl S-phenyl ester, also known as O-methyl S-phenyl ester of dithiocarbonic acid, is an organic compound with the chemical formula C8H9O2S2. It is a colorless to pale yellow liquid with a pungent odor. Dithiocarbonic acid O-methyl S-phenyl ester is derived from the esterification of dithiocarbonic acid with methanol and phenol, resulting in the formation of an O-methyl S-phenyl ester. It is used as a chemical intermediate in the synthesis of various organic compounds, particularly in the production of pesticides and pharmaceuticals. Due to its reactivity and potential toxicity, it is important to handle Dithiocarbonic acid O-methyl S-phenyl ester with care and in accordance with proper safety protocols.

6047-46-7

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6047-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6047-46-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6047-46:
(6*6)+(5*0)+(4*4)+(3*7)+(2*4)+(1*6)=87
87 % 10 = 7
So 6047-46-7 is a valid CAS Registry Number.

6047-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dithiocarbonic acid O-methyl ester-S-phenyl ester

1.2 Other means of identification

Product number -
Other names O-Methyl-S-phenyl-dithiocarbonat

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:6047-46-7 SDS

6047-46-7Downstream Products

6047-46-7Relevant academic research and scientific papers

Correlation of the rates of solvolysis of phenyl chlorothionoformate and phenyl chlorodithioformate

Kevill, Dennis N.,D'Souza, Malcolm J.

, p. 1118 - 1122 (2007/10/03)

The specific rates of solvolysis of phenyl chlorothionoformate (PhOCSCl) are remarkably similar to those previously reported for phenyl chlorothioformate (PhSCOCl). When analyzed using the extended Grunwald-Winstein equation over the usual range of solvent types, these solvolyses show essentially identical divisions into the solvents favoring the addition-elimination channel and those favoring the ionization channel. The introduction of one sulfur caused a partial shift away from the addition-elimination pathway, which was dominant over the full range of solvents for phenyl chloroformate (PhOCOCl). Consistent with these results, introduction of the second sulfur within phenyl chlorodithioformate (PhSCSCl) leads to a completion of this shift, such that an extended Grunwald-Winstein treatment of the specific rates of solvolysis now shows the ionization pathway to be dominant over the full range of solvents.

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