106748-14-5

Basic information

• Product Name: 5-Amino-1-(4-bromophenyl)-1H-1,2,3-triazole-4-carboxylicacid ethyl ester
• Synonyms: 5-Amino-1-(4-bromophenyl)-1H-1,2,3-triazole-4-carboxylicacid ethyl ester;5-Amino-1-(4-bromophenyl)-1H-1,2,3-triazole-4-carboxylic acid ethyl ester
• CAS NO: 106748-14-5
• Molecular Formula: C₁₁H₁₁BrN₄O₂
• Molecular Weight: 311.138
• Mol File: 106748-14-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-Amino-1-(4-bromophenyl)-1H-1,2,3-triazole-4-carboxylicacid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Amino-1-(4-bromophenyl)-1H-1,2,3-triazole-4-carboxylicacid ethyl ester(106748-14-5)
• EPA Substance Registry System: 5-Amino-1-(4-bromophenyl)-1H-1,2,3-triazole-4-carboxylicacid ethyl ester(106748-14-5)

Safety Data

• Hazardous Substances Data: 106748-14-5(Hazardous Substances Data)

Upstream product

• 2101-88-4 1-azido-4-bromobenzene 
• 105-56-6 ethyl 2-cyanoacetate 
• 137999-47-4 2-Ethoxycarbonyl-N-(4-bromophenyl)acetamidine hydrochloride 
• 13621-50-6 ethoxycarbonylthioacetamide 
• 5873-88-1 2-Ethoxycarbonyl-S-methylthioacetamidate hydrochloride 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 1160947-78-3 5-(4-bromophenylamino)-2-methylsulfanylmethyl-2H-1,2,3-triazol-4-carboxylic acid ethyl ester 

Relevant articles and documents

Synthesis and in vitro and in silico studies of 1H- and 2H-1,2,3-triazoles as antichagasic agents

1,2,3-triazole heterocycles stand out in medicinal chemistry for having great structural diversity and bioactivities. In this study, two series of triazoles were synthesized. One was obtained by the 1,3-dipolar cycloaddition reaction between ethyl cyanoac

COMPOUNDS AND METHODS FOR TREATING OXALATE-RELATED DISEASES

Disclosed herein are compounds and compositions for modulating glycolate oxidase, useful for treating oxalate-related diseases, such as hyperoxaluria, where modulating glycolate oxidase is expected to be therapeutic to a patent in need thereof. Methods of modulating glycolate oxidase activity in a human or animal subject are also provided.

NEW METHOD FOR STUDYING THE REACTIVITIES OF α-DIAZO IMINES. INVESTIGATION OF THE CYCLIZATION OF N-SUBSTITUTED 2-DIAZOACETAMIDINES TO 1,2,3-TRIAZOLES

N-Substituted diazoacetamidines were generated in the reaction of N-substituted acetamidines with benzenesulfonyl azide.It is shown that their cyclization to isomeric 1,2,3-triazole characterizes the reactivities of α-diazo imines.The synthesis of 5-amino