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75773-99-8

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75773-99-8 Usage

General Description

1H-Tetrazole-5-carboxylic acid is a heterocyclic compound with the chemical formula C3H2N4O2. It is a white to off-white crystalline powder that is soluble in water and organic solvents. 1H-Tetrazole-5-carboxylic acid is often used as a building block in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also used as a ligand in coordination chemistry and as a stabilizer in explosives. Additionally, 1H-Tetrazole-5-carboxylic acid has potential applications in the field of materials science, particularly in the development of novel polymers and coordination networks. Overall, this compound is a versatile and important chemical building block with a wide range of potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 75773-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75773-99:
(7*7)+(6*5)+(5*7)+(4*7)+(3*3)+(2*9)+(1*9)=178
178 % 10 = 8
So 75773-99-8 is a valid CAS Registry Number.

75773-99-8SDS

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 2H-tetrazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1H-Tetrazol-5-carbonsaeure

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:75773-99-8 SDS

75773-99-8Relevant articles and documents

8-Polycycloalkyl-1,3-dipropylxanthines as potent and selective antagonists for A1-adenosine receptors

Shimada,Suzuki,Nonaka,Ishii

, p. 924 - 930 (2007/10/02)

With the aim of characterizing the hydrophobic interactions between xanthines and the A1 receptor site, 1,3-dipropyl-8-substituted xanthines were synthesized. Introduction of a quaternary carbon and the conformationally restricted cyclopentyl moiety into the 8-position of xanthines enhanced the adenosine A1 antagonism. 1,3-Dipropyl-8-(3- noradamantyl)xanthine (42) was identified to be a selective and the most potent A1 receptor antagonist reported to date. Under our structure-activity relationship, the 8-substituent of xanthine antagonists and the N6- substituent of adenosine agonists appears to bind to the same region of the A1 receptor.

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