1113-62-8

Basic information

• Product Name: 3-Penten-2-one, 4-amino-3-methyl- (7CI,8CI,9CI)
• Synonyms: 4-Amino-3-methyl-3-penten-2-one;3-Penten-2-one, 4-amino-3-methyl- (7CI,8CI,9CI)
• CAS NO: 1113-62-8
• Molecular Formula: C₆H₁₁NO
• Molecular Weight: 113.15764
• Product Categories: ACETYLGROUP
• Mol File: 1113-62-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Penten-2-one, 4-amino-3-methyl- (7CI,8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Penten-2-one, 4-amino-3-methyl- (7CI,8CI,9CI)(1113-62-8)
• EPA Substance Registry System: 3-Penten-2-one, 4-amino-3-methyl- (7CI,8CI,9CI)(1113-62-8)

Safety Data

• Hazardous Substances Data: 1113-62-8(Hazardous Substances Data)

Upstream product

• 10557-82-1 3,4,5-trimethylisoxazole 
• 3002-24-2 hexane-2,4-dione 
• 815-57-6 3-Methyl-2,4-pentanedione 
• 60-29-7 diethyl ether 
• 1522-25-4 4-hydroxy-3-methylpent-3-en-2-one 
• 15435-71-9 sodium acetoacetonate 
• 123-54-6 acetylacetone 

Downstream Products

• 7664-41-7 ammonia 
• 64-19-7 acetic acid 
• 78-93-3 butanone 
• 91591-64-9 2-chloro-4,5,6-trimethylpyridine-3-carbonitrile 
• 17697-92-6 4,5,6-trimethyl-2,5-dihydro-2-thioxopyrimidine 
• 614-23-3 N-benzoylthiourea 
• 85741-87-3 N-benzoyl-N'-(1,2-dimethyl-3-oxo-1-butenyl)thiourea 
• 81818-60-2 1-Phenyl-4,5,6-trimethylpyrimidin-2(1H)-one 
• 26823-24-5 1-Phenyl-3-(1,2-dimethyl-3-oxo-1-butenyl)urea 

Relevant articles and documents

Molecular structure and intramolecular hydrogen bond strength of 3-methyl-4-amino-3-penten-2-one and its N–Me and N-Ph substitutions by experimental and theoretical methods

In the present work, molecular structures and intramolecular hydrogen bonding (IHB) of 3-methyl-4-amino-3-penten-2-one, 3-MeAPO, 3-methyl-4-methylamino-3-penten-2-one, 3-Me-MeAPO, and the 3-methyl-4-phenylamino-3-penten-2-one, 3-Me-PhAPO have been investi

Photocycloaddition of aromatic and aliphatic aldehydes to isoxazoles: Cycloaddition reactivity and stability studies

The first photocycloadditions of aromatic and aliphatic aldehydes to methylated isoxazoles are reported. The reactions lead solely to the exo-adducts with high regio- and diastereoselectivities. Ring methylation of the isoxazole substrates is crucial for high conversions and product stability. The 6-arylated bicyclic oxetanes 9a-9c were characterized by X-ray structure analyses and showed the highest thermal stabilities. All oxetanes formed from isoxazoles were highly acid-sensitive and also thermally unstable. Cleavage to the original substrates is dominant and the isoxazole derived oxetanes show type T photochromism.