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21743-64-6

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21743-64-6 Usage

Description

2H-tetrazol-2-acetic acid, a member of the tetrazole family, is a chemical compound with the molecular formula C3H4N4O2. It is known for its unique structure and properties, making it a valuable building block in the synthesis of various organic molecules, particularly in the development of new pharmaceuticals and other bioactive compounds.

Uses

Used in Pharmaceutical Synthesis:
2H-tetrazol-2-acetic acid is used as a precursor in the pharmaceutical industry for the synthesis of various organic compounds. Its unique structure and properties make it a valuable building block in the development of new drugs.
Used in Corrosion Inhibition:
2H-tetrazol-2-acetic acid is used as a corrosion inhibitor in industrial processes. Its potential as a stabilizer for metal ions helps protect materials from corrosion, extending their lifespan and improving their performance.
Used in Metal Ion Stabilization:
In industrial applications, 2H-tetrazol-2-acetic acid is used as a stabilizer for metal ions. Its ability to form stable complexes with metal ions contributes to the stability and performance of various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 21743-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21743-64:
(7*2)+(6*1)+(5*7)+(4*4)+(3*3)+(2*6)+(1*4)=96
96 % 10 = 6
So 21743-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H4N4O2/c8-3(9)1-7-5-2-4-6-7/h2H,1H2,(H,8,9)

21743-64-6SDS

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-(tetrazol-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-Tetrazolylacetic Acid

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:21743-64-6 SDS

21743-64-6Downstream Products

21743-64-6Relevant articles and documents

Preparation and characterization of the first coordination compounds of tetrazol-2-ylacetic acid

Voitekhovich, Sergei V.,Serebryanskaya, Tatiyana V.,Gaponik, Pavel N.,Ivashkevich, Ludmila S.,Lyakhov, Alexander S.,Ivashkevich, Oleg A.

, p. 949 - 951 (2010)

Tetrazol-2-ylacetic acid (2-TzaH) was found to react with CuCl2, PdCl2, and K2PtCl4 in water giving Cu(2-Tza)2, PdCl2(2-TzaH)2·2H2O and PtCl2(2-TzaH)2, correspondingly. Obtained complexes, being the first reported examples of coordination compounds derived from 2-TzaH, have been characterized by IR spectroscopy, thermal and X-ray diffraction methods. 2-TzaH was found to act as a monodentate ligand coordinated to the metal ion via N4 atom of heteroring in palladium complex and as tridentate bridging ligand coordinated via N4 atom and two oxygen atoms in copper complex. Cu(2-Tza)2 presents 2D coordination polymer, whereas PdCl2(2-TzaH)2·2H2O is molecular complex.

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