13788-89-1

Basic information

• Product Name: 4-phenylamino-3-buten-2-one
• Synonyms: 4-phenylamino-3-buten-2-one
• CAS NO: 13788-89-1
• Molecular Weight: 161.203
• Mol File: 13788-89-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-phenylamino-3-buten-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenylamino-3-buten-2-one(13788-89-1)
• EPA Substance Registry System: 4-phenylamino-3-buten-2-one(13788-89-1)

Safety Data

• Hazardous Substances Data: 13788-89-1(Hazardous Substances Data)

Upstream product

• 1119-19-3 but-2-ynal 
• 62-53-3 aniline 
• 67-64-1 acetone 
• 109-94-4 formic acid ethyl ester 
• 1190-91-6 4-dimethylamino-3-buten-2-one 
• 142-04-1 aniline hydrochloride 
• 106237-23-4 4-anilino-but-3-en-2-one-phenylimine 
• 13945-19-2 4-acetoxy-3-buten-2-one 

Downstream Products

• 128979-27-1 1-(1-phenyl-1H-1,2,3-triazol-4-yl)ethan-1-one 
• 5765-44-6 5-methylisoxazole 
• 102022-52-6 3,5-diacetyl-4-[2]furyl-1-phenyl-1,4-dihydro-pyridine 
• 79901-56-7 1-(3-Methyl-1-phenyl-1,2,3,4-tetrahydro-pyrimidin-5-yl)-ethanone 
• 79901-57-8 1-(3-tert-Butyl-1-phenyl-1,2,3,4-tetrahydro-pyrimidin-5-yl)-ethanone 
• 79901-19-2 (Z)-3-Dimethylaminomethyl-4-phenylamino-but-3-en-2-one 
• 79901-14-7 (E)-3-Dimethylaminomethyl-4-phenylamino-but-3-en-2-one 
• 79901-23-8 (Z)-3-Azepan-1-ylmethyl-4-phenylamino-but-3-en-2-one 
• 79901-18-1 (E)-3-Azepan-1-ylmethyl-4-phenylamino-but-3-en-2-one 
• 79901-22-7 (Z)-3-Morpholin-4-ylmethyl-4-phenylamino-but-3-en-2-one 
• 79901-17-0 (E)-3-Morpholin-4-ylmethyl-4-phenylamino-but-3-en-2-one 
• 79901-21-6 (Z)-4-Phenylamino-3-piperidin-1-ylmethyl-but-3-en-2-one 
• 79901-16-9 (E)-4-Phenylamino-3-piperidin-1-ylmethyl-but-3-en-2-one 
• 79901-20-5 (Z)-4-Phenylamino-3-pyrrolidin-1-ylmethyl-but-3-en-2-one 

Relevant articles and documents

Base-Promoted Synthesis of N-Substituted 1,2,3-Triazoles via Enaminone-Azide Cycloaddition Involving Regitz Diazo Transfer

The domino reactions between NH-based secondary enaminones and tosyl azide have been developed for the synthesis of various N-substituted 1,2,3-triazoles by employing t-BuONa as the base promoter. Through a key Regitz diazo-transfer process with tosyl azi