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191602-76-3

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191602-76-3 Usage

General Description

5-(3-Bromo-4-methoxy-phenyl)-2H-tetrazole is a chemical compound with the molecular formula C8H7BrN4O. It is a tetrazole derivative with a 3-bromo-4-methoxy-phenyl group attached to the tetrazole ring. 5-(3-BROMO-4-METHOXY-PHENYL)-2H-TETRAZOLE is commonly used in organic synthesis and pharmaceutical research, particularly in the development of potential drug candidates. It has been studied for its potential biological activities, including antimicrobial, antiviral, and anti-inflammatory properties. Additionally, it has been explored for its potential use in the development of new materials and in the improvement of existing products.

Check Digit Verification of cas no

The CAS Registry Mumber 191602-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,6,0 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 191602-76:
(8*1)+(7*9)+(6*1)+(5*6)+(4*0)+(3*2)+(2*7)+(1*6)=133
133 % 10 = 3
So 191602-76-3 is a valid CAS Registry Number.

191602-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-bromo-4-methoxyphenyl)-2H-tetrazole

1.2 Other means of identification

Product number -
Other names 5-(3-Bromo-4-methoxy-phenyl)-2H-tetrazole

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:191602-76-3 SDS

191602-76-3Downstream Products

191602-76-3Relevant articles and documents

Practical scale up synthesis of carboxylic acids and their bioisosteres 5-substituted-1H-tetrazoles catalyzed by a graphene oxide-based solid acid carbocatalyst

Mittal, Rupali,Kumar, Amit,Awasthi, Satish Kumar

, p. 11166 - 11176 (2021/03/31)

Herein, catalytic application of a metal-free sulfonic acid functionalized reduced graphene oxide (SA-rGO) material is reported for the synthesis of both carboxylic acids and their bioisosteres, 5-substituted-1H-tetrazoles. SA-rGO as a catalytic material incorporates the intriguing properties of graphene oxide material with additional benefits of highly acidic sites due to sulfonic acid groups. The oxidation of aldehydes to carboxylic acids could be efficiently achieved using H2O2as a green oxidant with high TOF values (9.06-9.89 h?1). The 5-substituted-1H-tetrazoles could also be effectively synthesized with high TOF values (12.08-16.96 h?1). The synthesis of 5-substituted-1H-tetrazoles was corroborated by single crystal X-ray analysis and computational calculations of the proposed reaction mechanism which correlated well with experimental findings. Both of the reactions could be performed efficiently at gram scale (10 g) using the SA-rGO catalyst. SA-rGO displays eminent reusability up to eight runs without significant decrease in its productivity. Thus, these features make SA-rGO riveting from an industrial perspective.

An efficient and economical synthesis of 5-substituted 1 H -tetrazoles via Pb(II) salt catalyzed [3+2] cycloaddition of nitriles and sodium azide

Kant, Rama,Singh, Vishal,Agarwal, Alka

, p. 305 - 312 (2016/04/20)

A simple, mild and efficient method is developed for the synthesis of 5-substituted 1H-tetrazoles. Out of three used Pb(II) catalysts, lead chloride (PbCl2) has been found to be an efficient catalyst for [3+2] cycloaddition of NaN3 with aromatic and aliphatic nitriles to afford 5-substituted 1H-tetrazoles. The catalyst is reusable up to four cycles with consistent activity. The cost effectiveness and easy availability of the catalyst, simple methodology, excellent yield and easy work-up are the additional advantages.

(NH4)2Ce(NO3)6 as an inexpensive, eco-friendly, efficient catalyst for the synthesis of 5-substituted 1-H tetrazoles from nitriles

Kumar, Satyanand,Dubey, Shristy,Saxena, Nisha,Awasthi, Satish Kumar

, p. 6034 - 6038 (2015/01/08)

Ceric ammonium nitrate (CAN) is found to be a suitable, inexpensive, and effective non-toxic catalyst for a smooth (3+2) cycloaddition of organic nitriles with NaN3 to afford 5-substituted 1H-tetrazoles in excellent yields. Shorter reaction times, easy work-up, and substantial and pure product formation are the key advantages of the present method.

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