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Thioacetic acid phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85033-96-1

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85033-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85033-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,3 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85033-96:
(7*8)+(6*5)+(5*0)+(4*3)+(3*3)+(2*9)+(1*6)=131
131 % 10 = 1
So 85033-96-1 is a valid CAS Registry Number.

85033-96-1SDS

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 Phenyl thionoacetate

1.2 Other means of identification

Product number -
Other names thioacetic acid O-phenyl 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:85033-96-1 SDS

85033-96-1Relevant academic research and scientific papers

Kinetics and Mechanism of the Aminolysis of Phenyl Thionoacetate in Aqueous Solution

Castro, Enrique A.,Ibanez, Fernando,Santos, Jose G.,Ureta, Carmen

, p. 4908 - 4912 (2007/10/02)

The reactions of a series of secondary alicyclic amines with the title substrate have been subjected to a kinetic study in water at 25 deg C, ionic strength 0.2 M.Pseudo-first-order rate coefficients (kobsd) are found throughout, under amine ex

Reduction of Thionoesters to Ethers by Triorganotin Hydrides

Smith, Colin,Tunstad, Linda M.,Gutierrez, Carlos G.

, p. 257 - 260 (2007/10/02)

Esters 1 are efficiently deoxygenated to the corresponding ethers 3 in two steps by first conversion to the thionoesters 2 and subsequent reduction of these by triorganotin hydrides.

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