99613-60-2

Basic information

• Product Name: 1H-1,2,3-Triazole-4-carboxamide, 5-amino-1-[(4-methylphenyl)methyl]-
• CAS NO: 99613-60-2
• Molecular Formula: C11H13N5O
• Molecular Weight: 231.257
• Mol File: 99613-60-2.mol

Chemical Properties

• CAS DataBase Reference: 1H-1,2,3-Triazole-4-carboxamide, 5-amino-1-[(4-methylphenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-Triazole-4-carboxamide, 5-amino-1-[(4-methylphenyl)methyl]-(99613-60-2)
• EPA Substance Registry System: 1H-1,2,3-Triazole-4-carboxamide, 5-amino-1-[(4-methylphenyl)methyl]-(99613-60-2)

Safety Data

• Hazardous Substances Data: 99613-60-2(Hazardous Substances Data)

Usage

Molecular structure

The compound is a derivative of 1,2,3-triazole with a carboxamide group and an amino group attached to the triazole ring, and a 4-methylphenylmethyl substituent.

Molecular weight

214.26 g/mol

Potential applications

The compound has potential applications in medicinal chemistry, such as in the development of pharmaceuticals or bioactive molecules.

Structure and properties

The unique arrangement of functional groups in the compound could potentially confer specific biological activities or interactions with biological targets.

Field of research

The compound is a promising candidate for further research and development in the field of drug discovery.

Upstream product

• 17271-89-5 4-methylphenylmethylazide 
• 107-91-5 cyanoacetic acid amide 
• 104-81-4 4-Methylbenzyl bromide 

Downstream Products

• 258356-24-0 [3-(4-methyl-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl]-hydrazine 
• 258356-19-3 3-(4-methyl-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-7-thiol 
• 258356-21-7 3-(4-methyl-benzyl)-7-methylsulfanyl-3H-[1,2,3]triazolo[4,5-d]pyrimidine 
• 258356-17-1 7-chloro-3-(4-methyl-benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine 
• 860470-50-4 3-(4-methyl-benzyl)-5-p-tolyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ylamine 
• 860470-45-7 3-(4-methyl-benzyl)-5-phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ylamine 
• 860470-37-7 3-(4-methyl-benzyl)-5-phenyl-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one 
• 860470-41-3 3-(4-methyl-benzyl)-5-p-tolyl-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one 
• 258356-16-0 3-(4-methyl-benzyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one 

Relevant articles and documents

2,9-Disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: Synthesis, biochemical and molecular modelling studies

A number of N6-(N-arylcarbamoyl)-2-substituted-9-benzyl-8- azaadenines, obtained by a modification of the synthetic scheme used to prepare selective A1 ligands, by only three or two steps, are described. At first we prepared a series

1,2,3-Triazolo[4,5-e]-1,2,4-triazolo[3,4-c]pyrimidines

Some new 1,2,3-triazolo[4,5-e]-1,2,4-triazolo[3,4-c]pyrimidines were prepared starting from the corresponding 1,2,3-triazolo[4,5-d]pyrimidines via the formation of the 1,2,4-triazole ring. Thus suitable hydrazino derivatives 6 were condensed with triethyl orthoformate, triethyl orthoacetate and triethyl orthobenzoate to give the expected tricyclic derivatives 7, 8 and 9. Intramolecular cyclization of the ethoxycarbonylhydrazino derivatives 10 gave the tricyclic compounds 11 bearing an hydroxyl group in the 3 position. The v-triazolo-s-triazolopyrimidine derivatives were tested towards the A1 and A(2A) adenosine receptors in binding assays, but they did not show any receptor affinity.

5-amino or substituted amino 1,2,3-triazoles

Novel 5-amino or substituted amino 1,2,3-triazoles are disclosed as having anticoccidial activity. The compounds are useful for controlling coccidiosis when administered in minor quantities to animals, in particular to poultry, usually in admixture with animal sustenance.