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193813-85-3

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193813-85-3 Usage

General Description

5-(2-Bromo-Benzyl)-2H-Tetrazole is a chemical compound with the molecular formula C8H7BrN4. It is an organic heterocyclic compound that contains a tetrazole ring with a benzyl group substituted at the 5-position and a bromine atom at the 2-position. 5-(2-BROMO-BENZYL)-2H-TETRAZOLE has been studied for its potential use in pharmaceutical research and drug development, particularly in the synthesis of novel pharmaceutical compounds and as a building block for heterocyclic derivatives. It is also used as a reagent in organic synthesis reactions and as a ligand in coordination chemistry. Additionally, 5-(2-Bromo-Benzyl)-2H-Tetrazole has potential applications in materials science and as a component in the synthesis of advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 193813-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,8,1 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 193813-85:
(8*1)+(7*9)+(6*3)+(5*8)+(4*1)+(3*3)+(2*8)+(1*5)=163
163 % 10 = 3
So 193813-85-3 is a valid CAS Registry Number.

193813-85-3SDS

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 5-(2-BROMO-BENZYL)-2H-TETRAZOLE

1.2 Other means of identification

Product number -
Other names -

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:193813-85-3 SDS

193813-85-3Downstream Products

193813-85-3Relevant articles and documents

Bioisosteres of 9-carboxymethyl-4-oxo-imidazo[1,2-a]indeno-[1,2-e]pyrazin-2-carboxylic acid derivatives. Progress towards selective, potent in vivo AMPA antagonists with longer durations of action

Jimonet, Patrick,Bohme, Georg Andrees,Bouquerel, Jean,Boireau, Alain,Damour, Dominique,Debono, Marc Williams,Genevois-Borella, Arielle,Hardy, Jean-Claude,Hubert, Philippe,Manfre, Franco,Nemecek, Patrick,Pratt, Jeremy,Randle, John C.R.,Ribeill, Yves,Stutzmann, Jean-Marie,Vuilhorgne, Marc,Mignani, Serge

, p. 127 - 132 (2007/10/03)

A novel series of 2- and 9-disubstituted heterocyclic-fused 4-oxo-indeno[1,2-e]pyrazin derivatives was synthesized. One of them, the 9-(1H-tetrazol-5-ylmethyl)-4-oxo-5,10-dihydroimidazo[1,2-a]indeno[1,2-e]pyraz in-2-yl phosphonic acid 4i exhibited a stron

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