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28996-51-2

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28996-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28996-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,9 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28996-51:
(7*2)+(6*8)+(5*9)+(4*9)+(3*6)+(2*5)+(1*1)=172
172 % 10 = 2
So 28996-51-2 is a valid CAS Registry Number.

28996-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzylidene-2-methylsulfanyl-1,3-thiazol-4-one

1.2 Other means of identification

Product number -
Other names 5-Benzyliden-2-methylthio-1,3-thiazolin-4-on

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:28996-51-2 SDS

28996-51-2Relevant articles and documents

ALKYLATION OF CRYSTALLINE 5-BENZYLIDENERHODANINE WITH DIAZOMETHANE

Ginak, A. I.,Rubleva, O. G.,Dymshits, V. A.

, p. 1184 (2007/10/02)

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REACTIVITY AND TAUTOMERISM OF AZOLIDINES. XLII. ALKYLATION OF THE ALKALI-METAL SALTS OF 5-BENZYLIDENERHODANINE IN THE SOLID PHASE.

V'yunov, K. A.,Ginak, A. I.,Ramsh, S. M.

, p. 192 - 194 (2007/10/02)

The effect of the counterion of the "leaving" group in the alkylating agent on the direction of alkylation in the alkali-metal salts of 5-benzylidenerhodanine in the solid phase was investigated.It was shown that the ratio of the isomeric products from alkylation at the N and S atoms varies with variation of the counterion and the substituted group in accordance with the principle of hard and soft acids and bases and increases in the series Li, Na, K, Cs.

REACTIVITY AND TAUTOMERISM OF AZOLIDINES. XXXII. THE EFFECT OF THE NATURE OF THE SOLVENT ON THE DUAL REACTIVITY OF 5-BENZYLIDENERHODANINE IN METHYLATION

Volkova, A. A.,V'yunov, K. A.,Ginak, A. I.,Ramsh, S. M.,Sochilin, E. G.

, p. 117 - 119 (2007/10/02)

The effect of the nature of the solvent on the dual reactivity of 5-benzylidenerhodanine in methylation was investigated.A correlation was obtained between the ratio of the rate constants for the reaction at the N and S centers of the substrate and the polarity of the solvent.Proposals are made concerning the mechanism of solvation of the ambident centers in 5-benzylidenerhodanine.

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