72806-73-6

Basic information

• Product Name: 2(3H)-Furanone, dihydro-5-methyl-3-(phenylmethylene)-, (3E)-
• CAS NO: 72806-73-6
• Molecular Formula: C12H12O2
• Molecular Weight: 188.226
• Mol File: 72806-73-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2(3H)-Furanone, dihydro-5-methyl-3-(phenylmethylene)-, (3E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Furanone, dihydro-5-methyl-3-(phenylmethylene)-, (3E)-(72806-73-6)
• EPA Substance Registry System: 2(3H)-Furanone, dihydro-5-methyl-3-(phenylmethylene)-, (3E)-(72806-73-6)

Safety Data

• Hazardous Substances Data: 72806-73-6(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 108-29-2 5-methyl-dihydro-furan-2-one 
• 6116-91-2 (E)-3-<2-(propen-2-yl)phenyl>propenoic acid 
• 26480-90-0 ethyl 2-(triphenyl-λ⁵-phosphanylidene)pent-4-enoate 
• 86725-67-9 (2-oxo-5-methyltetrahydrofuran-3-yl)-phosphonic acid diethyl ester 
• 172656-35-8 2-benzylidene-pent-4-enoic acid ethyl ester 
• 222718-21-0 methyl (E)-2-(2-oxopropyl)-3-phenylprop-2-enoate 
• 2117-11-5 4-pentyn-2-ol 
• 98158-55-5 methyl (E)-2-(benzylidene)pent-4-enoate 
• 112197-32-7 α-(diphenylmethylsilyl)-γ-valerolactone 
• 116145-49-4 2-(Bis-methylsulfanyl-methylene)-1-phenyl-pent-4-en-1-ol 
• 97510-25-3 2-(bis(methylthio)methylene)-1-phenylpent-4-en-1-one 
• 2833-24-1 methyl (E)-4-oxo-2-pentenoate 
• 622-42-4 1-nitro-1-phenylmethane 

Relevant articles and documents

Spiroaziridines from 4-substituted α-ylidene-γ-butyro lactones

4-Substituted α-ylidene-γ-butyrolactones produce N-ethoxycarbonyl-spiroaziridino γ-lactone diastereomers on treatment with NsONHCO2Et and CaO. A good stereofacial preference is observed when the ring substituent is a phenyl group. These product

A two steps synthesis of γ-substituted and γ,γ-disubstituted α-(alkylmethylene)-γ-butyrolactones

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POLARIZED KETENE DITHIOACETALS 63. STEREOSELECTIVE SYNTHESIS OF Α-YLIDENE-Γ-BUTYROLACTONES

A facile method for highly stereoselective synthesis of α-arylidene (4a-d, 4f-h and 4j) and α-ethylidene (4e,4i)-γ-butyrolactones has been developed by acid catalyzed lactonization of the corresponding α-ylidene-γ,δ-unsaturated esters 3a-j.The required es