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24433-71-4

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24433-71-4 Usage

Class

Tetrazole derivative

Structure

Five-membered ring containing four nitrogen atoms and one carbon atom

Industrial applications

Chemical intermediate, pharmaceutical synthesis

Unique properties

Useful in the production of pharmaceuticals and agrochemicals

Potential applications

Development of new materials, explosives

Safety concerns

Hazardous if not used and stored properly

Check Digit Verification of cas no

The CAS Registry Mumber 24433-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,3 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24433-71:
(7*2)+(6*4)+(5*4)+(4*3)+(3*3)+(2*7)+(1*1)=94
94 % 10 = 4
So 24433-71-4 is a valid CAS Registry Number.

24433-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Phenyl-tetrazol-1-ylamin

1.2 Other means of identification

Product number -
Other names 1-Ethyl-5-phenyl-tetrazol

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:24433-71-4 SDS

24433-71-4Relevant articles and documents

Preparation of 1,5-disubstituted tetrazoles under phase-transfer conditions

Artamonova,Zhivich,Dubinskii,Koldobskii

, p. 1428 - 1430 (2007/10/03)

Imidoyl chlorides, obtained by common methods from a wide range of aromatic mono- and diamides, are smoothly converted to the corresponding tetrazoles in high yields by treatment with NaN3 under phase-transfer conditions.

Novel regioselective N-alkylations of 5-substituted-2H-tetrazoles

Prhavc,Kobe

, p. 1925 - 1928 (2007/10/02)

Regioselective alkylation of 5-substituted-2H-tetrazoles 1 to 2-alkyl derivatives 3 was achieved via decarboxylative alkylation with alkyl cyanoformates. Lesser selectivity was observed with chloroformates.

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