4923-01-7 Usage
Uses
Used in Pharmaceutical Industry:
3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with diverse therapeutic properties.
Used in Agrochemical Industry:
In agrochemicals, 3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE serves as a key component in the creation of compounds designed to protect crops and enhance agricultural productivity.
Used as a Corrosion Inhibitor:
3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE is utilized as a corrosion inhibitor, helping to prevent the degradation of materials in various industrial applications, thereby extending their service life and improving efficiency.
Used as a Stabilizer in Photographic Emulsions:
3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE is employed as a stabilizer in photographic emulsions, ensuring the longevity and quality of photographic images by preventing unwanted chemical reactions.
Used in Dye Production:
3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE is used as an intermediate in the production of dyes, contributing to the synthesis of colorants for various applications, including textiles and printing inks.
Used in Antifungal, Antibacterial, and Antitumor Applications:
3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE has been studied for its potential biological activities, including its antifungal, antibacterial, and antitumor properties, indicating its potential use in the development of treatments for various diseases and infections.
Check Digit Verification of cas no
The CAS Registry Mumber 4923-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4923-01:
(6*4)+(5*9)+(4*2)+(3*3)+(2*0)+(1*1)=87
87 % 10 = 7
So 4923-01-7 is a valid CAS Registry Number.
4923-01-7Relevant articles and documents
NITROAZINES. XIV. AMBIDENT NATURE OF ARYLAMINES IN REACTIONS WITH 6-NITROAZOLOPYRIMIDINES
Rusinov, V. L.,Tumashov, A. A.,Pilicheva, T. L.,Chupakhin, O. N.
, p. 952 - 957 (2007/10/02)
During the reaction of 6-nitroazolopyrimidines with dialkylanilines the products from addition at the carbon atom, i.e., 6-nitro-7-p-dialkylaminophenyl-4,7-dihydroazolopyrimidines are formed.The reaction with aniline and its derivatives leads to destruction of the pyrimidine ring as a result of N-addition of the arylamine.
