74796-42-2

Basic information

• Product Name: E-2,2-dimethyl-5-(1-methyl-4-phenylbutadienyl)-3(2H)-furanone
• Synonyms: E-2,2-dimethyl-5-(1-methyl-4-phenylbutadienyl)-3(2H)-furanone
• CAS NO: 74796-42-2
• Molecular Weight: 254.329
• Mol File: 74796-42-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: E-2,2-dimethyl-5-(1-methyl-4-phenylbutadienyl)-3(2H)-furanone(CAS DataBase Reference)
• NIST Chemistry Reference: E-2,2-dimethyl-5-(1-methyl-4-phenylbutadienyl)-3(2H)-furanone(74796-42-2)
• EPA Substance Registry System: E-2,2-dimethyl-5-(1-methyl-4-phenylbutadienyl)-3(2H)-furanone(74796-42-2)

Safety Data

• Hazardous Substances Data: 74796-42-2(Hazardous Substances Data)

Upstream product

• 75767-43-0 2-methyl-2-<(trimethylsilyl)oxy>-3,5-heptanedione 
• 75767-42-9 5-hydroxy-2-methyl-2-<(trimethylsilyl)oxy>-3-heptanone 
• 55816-60-9 3-methyl-3-<(trimethylsilyl)oxy>-2-butanone 
• 18458-23-6 2,2-dimethyl-5-ethyl-furan-3(2H)-one 
• 14371-10-9 (E)-3-phenylpropenal 
• 136823-47-7 (E,E)-6-amino-3,7-dimethyl-1,7-dihydroxy-4-oxo-2,5-octadiene 
• 101417-83-8 5-<(E)-3-hydroxy-1-methyl-1-propenyl>-α,α-dimethyl-isoxazolemethanol 
• 87064-11-7 2,2-dimethyl-5-((E)-1-methyl-3-hydroxy-1-propenyl)-3(2H)-furanone 
• 110841-49-1 {1-[5-(1-Hydroxy-1-methyl-ethyl)-isoxazol-3-yl]-ethyl}-phosphonic acid diethyl ester 
• 110841-48-0 [5-(1-Hydroxy-1-methyl-ethyl)-isoxazol-3-ylmethyl]-phosphonic acid diethyl ester 
• 136823-60-4 2,2-dimethyl-5-<(E)-3-formyl-2-propen-2-yl>-3(2H)-furanone 
• 16721-45-2 triphenyl(phenylmethylene)phosphorane 
• 74796-29-5 2,2-dimethyl-5-(1-methyl-2-hydroxy-4-phenyl-3-butenyl)-3(2H)-furanone 
• 110841-44-6 [1-(5,5-Dimethyl-4-oxo-4,5-dihydro-furan-2-yl)-ethyl]-phosphonic acid diethyl ester 

Relevant articles and documents

Geiparvarin analogues. 2. Synthesis and cytostatic activity of 5-(4- arylbutadienyl)-3(2H)-furanones and of N-substituted 3-(4-oxo-2-furanyl)-2- buten-2-yl carbamates

In an attempt to determine some of the structural features of geiparvarin (1) that account for its cytostatic activity in vitro, a series of geiparvarin analogues (10a-i, l, 12, and 14-16) which contain novel modifications in the region of the olefinic do

Synthesis and Configurational Assignment of Geiparvarin: A Novel Antitumor Agent

This report presents the first total synthesis of geiparvarin as well as assignment of configuration of the previously undefined trisubstituted olefin.A central aspect of this synthetic adventure leading to this novel antitumor agent which possesses the 3