1255952-14-7

Basic information

• Product Name: 4-(2-azido-phenyl)-but-3-en-2-one
• Synonyms: 4-(2-azido-phenyl)-but-3-en-2-one
• CAS NO: 1255952-14-7
• Molecular Weight: 187.201
• Mol File: 1255952-14-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-(2-azido-phenyl)-but-3-en-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-azido-phenyl)-but-3-en-2-one(1255952-14-7)
• EPA Substance Registry System: 4-(2-azido-phenyl)-but-3-en-2-one(1255952-14-7)

Safety Data

• Hazardous Substances Data: 1255952-14-7(Hazardous Substances Data)

Upstream product

• 16714-25-3 2-azidobenzaldehyde 
• 67-64-1 acetone 
• 552-89-6 2-nitro-benzaldehyde 
• 1439-36-7 1-triphenylphosphoranylidene-2-propanone 

Downstream Products

• 703-80-0 3-acetylindole 
• 91-63-4 2-methylquinoline 
• 4264-35-1 2-acetylindole 
• 1355466-34-0 1-(3-(4-fluorophenyl)-3,4-dihydro-2-(1H-imidazol-1-yl)-quinazolin-4-yl)propan-2-one 
• 1355466-30-6 1-(3-(4-chlorophenyl)-3,4-dihydro-2-(1H-imidazol-1-yl)-quinazolin-4-yl)propan-2-one 
• 1422541-92-1 1-(3,4-dihydro-3-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)quinazolin-4-yl)propan-2-one 
• 1422541-91-0 1-(3,4-dihydro-3-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-yl)quinazolin-4-yl)propan-2-one 
• 1422541-90-9 1-(3,4-dihydro-3-m-tolyl-2-(1H-1,2,4-triazol-1-yl)quinazolin-4-yl)propan-2-one 
• 1422541-89-6 1-(3,4-dihydro-3-phenyl-2-(1H-1,2,4-triazol-1-yl)quinazolin-4-yl)-propan-2-one 
• 1355466-28-2 1-(3-phenyl-3,4-dihydro-2-(1H-imidazol-1-yl)quinazolin-4-yl)-propan-2-one 

Relevant articles and documents

An Efficient Protocol for the Synthesis of Pyrazolo[1,5- c ]quinazolines by a Staudinger-Aza-Wittig-Dehydroaromatization Sequence

The one-pot synthesis of azide-substituted dihydropyrazoles in isopropanol was performed by using chalcones, hydrazine hydrate, and an acyl chloride at 0 . Subsequent Staudinger aza-Wittig dehydroaromatization reactions of the products with methyl(dipheny

Synthesis of 2H-pyrrolo[3,4-C]quinoline via an Aldol/Van Leusen/Staudinger/aza-Wittig sequence

An aldol/van Leusen/Staudinger/aza-Wittig reaction for the preparation of the derivatives of 2H-pyrrolo[3,4-c]quinolines from 2-azidobenzaldehyde, acetyl compounds, and tosylmethyl isocyanide was developed. The process involves an aldol condensation of 2-