72470-51-0 Usage
Usage
Pharmaceutical industry building block
Utilized as an intermediate compound in the synthesis of various drug molecules.
Class
Benzoic acids
A classification of organic compounds consisting of a carboxylic acid group (-COOH) attached to a benzene ring.
Structural Feature
Tetrazole ring
A heterocyclic ring consisting of four nitrogen atoms and one carbon atom, contributing to the compound's chemical properties and reactivity.
Potential Applications
Anti-inflammatory, antimicrobial, and anticancer drugs
Due to its pharmacological properties, the compound may be used in the development of medications targeting inflammation, infections, and cancer.
Usage as a Reagent
Organic synthesis and medicinal chemistry research
The compound serves as a reagent in chemical reactions to facilitate the synthesis of other organic molecules and pharmaceuticals.
Possible Applications in Other Fields
Materials science and agriculture
2-(5-methyl-1H-tetraazol-1-yl)benzoic acid may have potential uses in developing new materials or agricultural products due to its unique chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 72470-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,7 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72470-51:
(7*7)+(6*2)+(5*4)+(4*7)+(3*0)+(2*5)+(1*1)=120
120 % 10 = 0
So 72470-51-0 is a valid CAS Registry Number.
72470-51-0Relevant academic research and scientific papers
Process for reparing imidazoquinolinamines
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, (2008/06/13)
A process for preparing 1H-imidazo?4,5-c!quinolin-4-amines is disclosed. The process involves reacting a 6H-imidazo?4,5-c!tetrazolo?1,5-a!quinoline with triphenylphosphine and hydrolyzing the product thereof.
Process for preparing tetrahdroimidazoquinolinamines
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, (2008/06/13)
A process for preparing 6, 7, 8, 9-tetrahydro-1H-imidazo?4,5-c!quinolin-4-amines is disclosed. The process involves the reduction of a 1H-imidazo?4,5-c!quinolin-4-amine or of a 6H-imidazo?4,5-c!tetrazolo?1,5-a!quinoline.
HETEROCYCLIZATION OF 1-(2'-CARBETHOXYPHENYL)-5-METHYLTETRAZOLE
Zyryanov, V. A.,Rusinov, V. L.,Postovskii, I. Ya.
, p. 1286 - 1288 (2007/10/02)
1-(2'-Carbethoxyphenyl)-5-methyltetrazole is converted to 5-hydroxytetrazolo-quinoline when it is heated in dimethylsulfoxide and dimethylformamide with sodium ethoxide.The hydroxy structure of the compound obtained was confirmed by spectral methods.
