22863-24-7

Basic information

• Product Name: 2,4-Dihydro-5-methyl-2-phenyl-3H-1,2,4-triazol-3-one
• Synonyms: 2,4-Dihydro-5-methyl-2-phenyl-3H-1,2,4-triazol-3-one;3H-1,2,4-Triazol-3-one, 2,4-dihydro-5-methyl-2-phenyl-;5-methyl-2-phenyl-1H-1,2,4-triazol-3-one
• CAS NO: 22863-24-7
• Molecular Formula: C₉H₉N₃O
• Molecular Weight: 175.19
• Mol File: 22863-24-7.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4-Dihydro-5-methyl-2-phenyl-3H-1,2,4-triazol-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Dihydro-5-methyl-2-phenyl-3H-1,2,4-triazol-3-one(22863-24-7)
• EPA Substance Registry System: 2,4-Dihydro-5-methyl-2-phenyl-3H-1,2,4-triazol-3-one(22863-24-7)

Safety Data

• Hazardous Substances Data: 22863-24-7(Hazardous Substances Data)

Usage

General Description

2,4-Dihydro-5-methyl-2-phenyl-3H-1,2,4-triazol-3-one, also known as DMT, is a synthetic organic compound with a molecular formula C10H10N2O. It is a white, crystalline solid with a molecular weight of 174.20 g/mol. This chemical is used primarily as a building block in the synthesis of other pharmaceutical compounds and agrochemicals. It has potential applications in the field of medicine, particularly in the development of new drugs to treat various diseases. DMT may also have uses in the agricultural industry as a pesticide or herbicide. However, its exact properties and potential uses are still being researched and explored.

Upstream product

• 133902-70-2 4-acetyl-1-phenyl-3,3-dimethyl-1,2,4-triazolidin-5-one 
• 5330-70-1 pyruvic acid phenylhydrazone 
• 31084-70-5 N-(1-Ethoxyethyliden)carbamidsaeure-ethylester 
• 100-63-0 phenylhydrazine 
• 62-53-3 aniline 
• 917-61-3 sodium isocyanate 
• 75-07-0 acetaldehyde 
• 28740-63-8 5-methyl-3-phenyl-1,3,4-oxadiazol-2(3H)-one 
• 2597-54-8 ethyl acetylcarbamate 
• 59-88-1 phenylhydrazine hydrochloride 
• 1445-45-0 Trimethyl orthoacetate 
• 7732-18-5 water 
• 7647-01-0 hydrogenchloride 
• 127-09-3 sodium acetate 

Downstream Products

• 43057-55-2 5-methyl-2-phenyl-1,2-dihydro-[1,2,4]triazole-3-thione 
• 948351-04-0 4-(4-bromo-3-methyl-benzyl)-5-methyl-2-phenyl-2,4-dihydro-[1,2,4]triazol-3-one 
• 111992-16-6 4,5-dihydro-3-methyl-4-difluoromethyl-1-(2,4-dichlorophenyl)-1,2,4-triazol-5(1H)-one 
• 122836-35-5 sulfentrazone 
• 111992-17-7 4,5-dihydro-3-methyl-4-difluoromethyl-1-(2,4-dichloro-5-nitrophenyl)-1,2,4-triazole-5(1H)-one 
• 111992-18-8 2-(5-amino-2,4-dichlorophenyl)-4-(difluoromethyl)-2,4-dihydro-5-methyl-3H-1,2,4-triazol-3-one 
• 133840-72-9 4,5-dihydro-3-methyl-1-(4-chlorophenyl)-1,2,4-triazol-5(1H)-one 
• 22863-25-8 5-methyl-2-(4-nitro-phenyl)-1,2-dihydro-[1,2,4]triazol-3-one 
• 34243-08-8 5-oxo-1-phenyl-2,5-dihydro-1H-[1,2,4]triazole-3-carboxylic acid 
• 90537-59-0 5-chloro-3-methyl-1-phenyl-1H-[1,2,4]triazole 
• 43057-60-9 3-methyl-1-phenyl-1H-1,2,4-triazole 
• 28740-67-2 4-Acetyl-3-methyl-1-phenyl-Δ²-1,2,4-triazolin-5-on 

Relevant articles and documents

Preparation method of 1-(2,4-dichlorophenyl)-4-difluoromethyl-3-methyl-1H-1,2,4-triazole-5-one

The invention provides a preparation method of 1-(2,4-dichlorophenyl)-4-difluoromethyl-3-methyl-1H-1,2,4-triazole-5-one. The method comprises the steps: taking aniline as a raw material; reducing witha catalyst X to prepare phenylhydrazine; under the action of acetaldehyde and sodium cyanate, carrying out cyclization on phenylhydrazine to generate 1-phenyl-3-methyl-1H-1,2,4-triazole-5-one; carrying out a reaction on 1-phenyl-3-methyl-1H-1,2,4-triazole-5-one and monochlorodifluoromethane under the action of a catalyst Y to generate 1-phenyl-3-methyl-4-difluoromethyl-1H-1,2,4-triazole-5-one, and carrying out catalytic chlorination through a catalyst Z to prepare 1-(2,4-dichlorophenyl)-4-difluoromethyl-3-methyl-1H-1,2,4-triazole-5-one.

C5-Alkyl-1,3,4-Oxadiazol-2-ones Undergo Dealkylation upon Nitrogen Insertion to Form 2H-1,2,4-Triazol-3-ones: Synthesis of 1,2,4-Triazol-3-one Hybrids with Triazolothiadiazoles and Triazolothiadiazines

The present study emphasizes on the dealklylation of 3-aryl-5-alkyl-2-oxo-Δ4-1,3,4-oxadiazoles when reacted with formamide resulting in the formation of 2-aryl-2H-1,2,4-triazol-3(4H)-ones as major product. Subsequent reactions of 2-aryl-2H-1,2,

Method of preparing aryl triazolinones with trialkyl orthoacetates

A method for preparing an alkoxyethylidene-substituted aryl hydrazine having the formula STR1 and thereafter cyclizing the same with a cyanate salt under mildly acidic conditions in the presence of an organic solvent, optionally in the presence of a cycli