1453164-22-1

Basic information

• Product Name: 1-(3-azidoprop-1-yn-1-yl)-4-methylbenzene
• Synonyms: 1-(3-azidoprop-1-yn-1-yl)-4-methylbenzene
• CAS NO: 1453164-22-1
• Molecular Weight: 171.202
• Mol File: 1453164-22-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(3-azidoprop-1-yn-1-yl)-4-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-azidoprop-1-yn-1-yl)-4-methylbenzene(1453164-22-1)
• EPA Substance Registry System: 1-(3-azidoprop-1-yn-1-yl)-4-methylbenzene(1453164-22-1)

Safety Data

• Hazardous Substances Data: 1453164-22-1(Hazardous Substances Data)

Upstream product

• 16017-25-7 3-(4-methylphenyl)- and 3-(4-methoxyphenyl)propargyl chloride 
• 16017-24-6 3-p-tolylprop-2-yn-1-ol 
• 1041791-61-0 C₁₁H₁₂O₃S 
• 624-31-7 4-tolyl iodide 

Downstream Products

• 1428257-22-0 1-azido-3-p-tolylprop-2-ynyl pivalate 
• 151589-34-3 3-(4-methylphenyl)-2-propynenitrile 
• 16017-26-8 3-(4-methylphenyl)prop-2-yn-1-amine 

Relevant articles and documents

Intercepting the Banert cascade with nucleophilic fluorine: Direct access to α-fluorinated: N H-1,2,3-triazoles

The treatment of propargylic azides with silver(i) fluoride in acetonitrile was found to yield α-fluorinated NH-1,2,3-triazoles via the Banert cascade. The reaction was regioselective and the products result from an initial [3,3] rearrangement. The reacti

One-Pot Synthesis of Polysubstituted Imidazoles via Sequential Staudinger/aza-Wittig/Ag(I)-Catalyzed Cyclization/Isomerization

A new one-pot preparation of polysubstituted imidazoles by a Staudinger/aza-Wittig/Ag(I)-catalyzed cyclization/isomerization has been developed. The easily accessible propargylazide derivatives reacted with triphenylphosphine, isocyanates, and amines sequ