1313994-71-6

Basic information

• Product Name: butyl-carbamic acid 1-benzyl-1H-[1,2,3]triazol-4-ylmethyl ester
• Synonyms: butyl-carbamic acid 1-benzyl-1H-[1,2,3]triazol-4-ylmethyl ester
• CAS NO: 1313994-71-6
• Molecular Weight: 288.349
• Mol File: 1313994-71-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: butyl-carbamic acid 1-benzyl-1H-[1,2,3]triazol-4-ylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: butyl-carbamic acid 1-benzyl-1H-[1,2,3]triazol-4-ylmethyl ester(1313994-71-6)
• EPA Substance Registry System: butyl-carbamic acid 1-benzyl-1H-[1,2,3]triazol-4-ylmethyl ester(1313994-71-6)

Safety Data

• Hazardous Substances Data: 1313994-71-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 622-79-7 benzyl azide 
• 76114-73-3 butylcarbamic acid prop-2-ynyl ester 

Relevant articles and documents

Alkyne-azide cycloaddition catalyzed by Fe-Cu nanoparticles

1,2,3-triazoles were synthesized using several alkynes and azides as starting materials in the presence of catalytic amounts of Cu-Fe nanoparticles. The process represents many advantages because it does not require additional bases or reductants, and thi

Catalytic activity of dithioic acid copper complexes in the alkyne-azide cycloaddition

Diverse dithioic acid copper complexes exhibit a high catalytic activity in the copper-catalyzed alkyne-azide cycloaddition using several solvents under different temperatures, showing a high efficiency with only 0.005 mmol catalyst/mmol alkyne or less. A dithioic acid copper complex derived from acetophenone was selected and used as the catalyst in the preparation of a library of 1,4-disubstituted-1,2,3-triazoles. This process occurred in high yields and good functional group tolerance.

Effect of temperature on triazole and bistriazole formation through copper-catalyzed alkyne-azide cycloaddition

Temperature is an important factor in the copper catalyzed alkyne azide cycloaddition under oxidative conditions. 1,2,3-Triazoles were obtained in high yields when several alkynes and azides were reacted at methanol reflux using catalytic amounts of both