5-Amino-1-benzyl-1H-1,2,3-triazole-4-carboxylic acid

Base Information

• Chemical Name: 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carboxylic acid
• CAS No.: 25784-56-9
• Molecular Formula: C10H10 N4 O2
• Molecular Weight: 218.212
• Hs Code.: 2933990090
• Mol file: 25784-56-9.mol

Synonyms:1H-1,2,3-Triazole-4-carboxylicacid, 5-amino-1-benzyl- (6CI,8CI); NSC 14768

Chemical Property of 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carboxylic acid

Chemical Property:

• Vapor Pressure: 5.56E-11mmHg at 25°C
• Boiling Point: 504°Cat760mmHg
• PKA: 3.65±0.50(Predicted)
• Flash Point: 258.6°C
• PSA: 94.03000
• Density: 1.47g/cm³
• LogP: 1.18800

Purity/Quality:

98%min ^*data from raw suppliers

5-amino-1-benzyl-1H-1,2,3-triazole-4-carboxylicAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carboxylic acid

There total 2 articles about 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

cyanoacetic acid (372-09-8) + benzyl azide (622-79-7) → 4-amino-3-benzyl-1,2,3-triazole-5-carboxylic acid (25784-56-9)

Guidance literature:

With sodium ethanolate;

DOI:10.1021/ja01603a033

Reference yield:

→ 4-amino-3-benzyl-1,2,3-triazole-5-carboxylic acid (25784-56-9)

Guidance literature:

aus Amid Ia;

DOI:10.1039/j39700000230

Reference yield: 79.0%

4-amino-3-benzyl-1,2,3-triazole-5-carboxylic acid (25784-56-9) + dicyclohexyl-carbodiimide (538-75-0) → cyclohexylamino(cyclohexylimino)methyl 5-amino-1-benzyl-1,2,3-triazole-4-carboxylate

Guidance literature:

With aniline; In acetonitrile; for 2h; Heating;

DOI:10.1023/A:1026004720790

upstream raw materials:

cyanoacetic acid

benzyl azide

Downstream raw materials:

1-benzyl-1H-1,2,3-triazol-5-amine

3-(2-((1-benzyl-1H-1,2,3-triazol-5-yl)amino)-5-chlorobenzylidene)cyclobutanecarboxylic acid

3-{2-[(1-benzyl-1H-1,2,3-triazol-5-yl)amino]-5-chlorophenyl}-2,2-dimethylpropanoic acid

[2-[(3-benzyltriazol-4-yl)amino]-5-chlorophenyl]methanol

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