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Benzamide, N-[4-(1H-tetrazol-5-yl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

651769-73-2

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651769-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651769-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,7,6 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 651769-73:
(8*6)+(7*5)+(6*1)+(5*7)+(4*6)+(3*9)+(2*7)+(1*3)=192
192 % 10 = 2
So 651769-73-2 is a valid CAS Registry Number.

651769-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(2H-tetrazol-5-yl)phenyl]benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-[4-(1H-tetrazol-5-yl)phenyl]

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:651769-73-2 SDS

651769-73-2Upstream product

651769-73-2Downstream Products

651769-73-2Relevant academic research and scientific papers

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.

AgNO3 catalyzed synthesis of 5-substituted-1H-tetrazole via [3+2] cycloaddition of nitriles and sodium azide Dedicated to the memory of late Dr. Tarkeshwar Gupta

Mani, Pavnesh,Singh, Ashawani Kumar,Awasthi, Satish Kumar

, p. 1879 - 1882 (2014/03/21)

An efficient one-pot, convenient catalysis for the synthesis of 5-substituted-1H-tetrazoles is reported. The [3+2] cycloaddition involves various nitriles, sodium azide in refluxing DMF and AgNO3 as catalyst to give corresponding 5-substituted-

Efficient heterogeneous silver nanoparticles catalyzed one-pot synthesis of 5-substituted 1H-tetrazoles

Mani, Pavnesh,Sharma, Chiranjeev,Kumar, Satyanand,Awasthi, Satish Kumar

, p. 150 - 156 (2014/06/23)

Silver nanoparticles (AgNPs), characterized by TEM, EDX and UV studies were used as an efficient heterogeneous catalyst for the synthesis of 5-substituted 1H-tetrazoles from various nitriles possessing different functional groups in excellent yields. All

5-Aryltetrazole Compounds, compositions thereof, and uses therefor

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Page 30, (2008/06/13)

The present invention relates to 5-Aryltetrazole compounds, compositions comprising a 5-Aryltetrazole compound, and methods for treating an inflammation disease, a reperfusion disease, hyperuricemia, gout, or tumor-lysis syndrome in an animal in need ther

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