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2,4(3H,5H)-Thiophenedione, 3-acetyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60700-15-4

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60700-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60700-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,0 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60700-15:
(7*6)+(6*0)+(5*7)+(4*0)+(3*0)+(2*1)+(1*5)=84
84 % 10 = 4
So 60700-15-4 is a valid CAS Registry Number.

60700-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-acetylthiolane-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-Acetyl-thiophen-2,4-dion

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:60700-15-4 SDS

60700-15-4Relevant academic research and scientific papers

Synthesis of endocyclic enol methyl ethers of 3-acylthiotetronic acids and their reactions with amines

Budnikova,Rubinov

, p. 1478 - 1485 (2007/10/03)

Acylation of (3H,5H)-tetrahydrothiophene-2,4-dione (thiotetronic acid) with acetyl, propionyl, and valeryl chlorides followed by O-C isomerization in the presence of 4-dimethylaminopyridine or acetone cyanohydrin gave rise to 3-acetyl, 3-propanoyl, and 3-pentanoyl derivatives of thiotetronic acid. The reaction of 3-acylthiotetronic acids with diazomethane afforded enol methyl ethers at the endocyclic keto groups. The subsequent reaction of these enol ethers with allylamine, benzylamine, and p-anisidine occurs along the mechanism of vinylog substitution providing the corresponding endocyclic enamino derivatives.

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