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Propanedinitrile, 2-thiazolyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71681-34-0

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71681-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71681-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,8 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71681-34:
(7*7)+(6*1)+(5*6)+(4*8)+(3*1)+(2*3)+(1*4)=130
130 % 10 = 0
So 71681-34-0 is a valid CAS Registry Number.

71681-34-0SDS

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 2-(1,3-thiazol-2-yl)malononitrile

1.2 Other means of identification

Product number -
Other names 2-Thiazol-2-yl-malononitrile

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:71681-34-0 SDS

71681-34-0Downstream Products

71681-34-0Relevant academic research and scientific papers

Substituted pyrazole derivatives condensed with six-membered heterocyclic rings

-

Page column 40, (2010/02/07)

The present invention relates to novel substituted pyrazole derivatives of the general formula (I) in which R1, R2, R3and A are each as defined, and to processes for their preparation and to their use as medicaments, in pa

ON THE REACTIVITY OF HALO-1,3-AZOLES AND RELATED COMPOUNDS TOWARD AROMATIC SN2 SUBSTITUTION

Yamanaka, Hiroshi,Ohba, Setsuya,Sakamoto, Takao

, p. 1115 - 1127 (2007/10/02)

Nucleophilic addition-elimination reactions of 2-methylsulfonyl-1,3-azoles with active methylene compounds were investigated in order to compare the reactivity of substrates.The order of oxazole > thiazole >> N-methylimidazole in the reactivity was exhibited clearly.Furthermore, in oxazole and thiazole series, the predominant reactivity of the 2-position over the 4- and 5-positions was indicated on the reaction with the carbanions generated from active methylene compounds.

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