4923-01-7

Basic information

• Product Name: 3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE
• Synonyms: 5-METHYL-4H-1,2,4-TRIAZOL-3-AMINE;5-METHYL-4H-[1,2,4]TRIAZOL-3-YLAMINE;(5-METHYL-4H-1,2,4-TRIAZOLE-3-YL)AMINE;3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE;3-AMINO-5-METHYL-1,2,4-TRIAZOLE;1H-1,2,4-triazol-3-aMine, 5-Methyl-;5-Methyl-4H-1,2,4-triazol-3-ylamine hydrochloride;5-Methyl-1H-[1,2,4]triazol-3-ylaMine
• CAS NO: 4923-01-7
• Molecular Formula: C₃H₆N₄
• Molecular Weight: 98.11
• Mol File: 4923-01-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: 142-144
• Boiling Point: 345.5°Cat760mmHg
• Flash Point: 189.6°C
• Appearance: /
• Density: 1.348g/cm³
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 11.56±0.40(Predicted)
• CAS DataBase Reference: 3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE(4923-01-7)
• EPA Substance Registry System: 3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE(4923-01-7)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 20/21/22-22
• Safety Statements: 22-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 4923-01-7(Hazardous Substances Data)

Usage

General Description

3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE is a chemical compound with the molecular formula C4H7N3. It is a heterocyclic organic compound that contains a triazole ring with an amino group at the 3-position and a methyl group at the 5-position. 3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It can also be used as a corrosion inhibitor, a stabilizer in photographic emulsions, and as an intermediate in the production of dyes. In addition, 3-AMINO-5-METHYL-4H-1,2,4-TRIAZOLE has been studied for its potential biological activities, including antifungal, antibacterial, and antitumor properties. Overall, this compound has a wide range of applications in various industries due to its versatile chemical structure and potential biological activities.

Upstream product

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Downstream Products

• 89852-99-3 2,5-dimethyl-1,2,4-triazolo<1,5-a>-7(4H)-pyrimidone 
• 117134-99-3 6-cyano-7,8-dihydro-2-methyl-5-phenyl-s-triazolo<1,5-a>pyrimidin-7-one 
• 115714-55-1 N-(3-methyl-1,2,4-triazolo-5-yl)-N'-benzoylthiourea 
• 1116117-24-8 2,7-dimethyl-6-phenyl[1,2,4]triazolo[1,5-a]pyrimidine-5-ol 
• 1116117-17-9 2-methyl-6-phenyl[1,2,4]triazolo[1,5-a]pyrimidine-5,7-diol 
• 168152-33-8 4'-[(2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]biphenyl-2-carbonitrile 
• 1239269-45-4 4'-[(7-butyl-5-oxo-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)methyl]-3',5'-difluorobiphenyl-2-carbonitrile 
• 1239269-94-3 4'-{[4-(2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylpropyl)-2-methyl-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile 
• 1250444-41-7 6-bromo-2-methyl-[1,2,4]triazolo[1,5-a]pyrimidine 
• 30302-88-6 2-Methyl-5,6-diphenyl-4H-imidazo[1,2-b][1,2,4]triazole 
• 117135-09-8 5-amino-1-desyl-3-methyl-s-triazole 
• 1335027-20-7 6-(3-chlorobenzyl)-5-cyclopropyl[1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one 

Relevant articles and documents

NITROAZINES. XIV. AMBIDENT NATURE OF ARYLAMINES IN REACTIONS WITH 6-NITROAZOLOPYRIMIDINES

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.