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75773-99-8

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75773-99-8 Usage

Description

1H-Tetrazole-5-carboxylic acid is a heterocyclic compound characterized by the chemical formula C3H2N4O2. It presents as a white to off-white crystalline powder that exhibits solubility in both water and organic solvents. This versatile chemical building block is known for its wide range of potential applications across different industries.

Uses

Used in Pharmaceutical Industry:
1H-Tetrazole-5-carboxylic acid is utilized as a key building block in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 1H-Tetrazole-5-carboxylic acid serves as an essential component in the creation of pesticides and other agricultural chemicals. Its incorporation enhances the effectiveness of these products, contributing to improved crop protection and yield.
Used in Dye Industry:
1H-Tetrazole-5-carboxylic acid is employed as a building block in the synthesis of dyes, imparting vibrant colors and improved properties to the final products. Its use in this industry contributes to the development of a diverse range of dyes for various applications.
Used in Coordination Chemistry:
As a ligand in coordination chemistry, 1H-Tetrazole-5-carboxylic acid plays a crucial role in the formation of coordination compounds. Its ability to bind with metal ions allows for the creation of complexes with specific properties and potential uses in various fields.
Used in Explosives Industry:
1H-Tetrazole-5-carboxylic acid is used as a stabilizer in the production of explosives. Its presence helps to ensure the safety and reliability of these materials, making it an important component in this high-risk industry.
Used in Materials Science:
In the realm of materials science, 1H-Tetrazole-5-carboxylic acid has potential applications in the development of novel polymers and coordination networks. Its unique properties and reactivity contribute to the advancement of new materials with specialized characteristics and uses.

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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