51384-73-7

Basic information

• Product Name: 3-Penten-2-one, 4-phenyl-, (Z)-
• Synonyms: 3-Penten-2-one,4-phenyl
• CAS NO: 51384-73-7
• Molecular Formula: C11H12O
• Molecular Weight: 160.216
• Mol File: 51384-73-7.mol
• Article Data: 19

Chemical Properties

• Boiling Point: 130 °C(Press: 12 Torr)
• Density: 0.997 g/cm3
• CAS DataBase Reference: 3-Penten-2-one, 4-phenyl-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Penten-2-one, 4-phenyl-, (Z)-(51384-73-7)
• EPA Substance Registry System: 3-Penten-2-one, 4-phenyl-, (Z)-(51384-73-7)

Safety Data

• Hazardous Substances Data: 51384-73-7(Hazardous Substances Data)

Upstream product

• 917-54-4 methyllithium 
• 20698-78-6 (+/-)-3-Methoxy-3-phenyl-buttersaeure 
• 1067-71-6 Diethyl (2-oxopropyl)phosphonate 
• 98-86-2 acetophenone 
• 1817-57-8 4-phenyl-3-butyne-2-one 
• 5158-46-3 methylzinc chloride 
• 108-24-7 acetic anhydride 
• 77202-09-6 4,6-dimethyl-1,2,3-triazine 
• 591-51-5 phenyllithium 
• 78840-02-5 2-phenyl-4-phenylthio-2-pentene 
• 78840-03-6 2-phenyl-4-ethylthio-2-pentene 
• 67262-97-9 4-dimethyl(phenyl)silyl-4-phenylpentan-2-one 
• 1067-88-5 diethyl phosphorylpropyne 
• 18854-62-1 3-Methyl-3-phnenylperlaevulincarbonsaeure-tert.-butylester 

Downstream Products

• 856-15-5 4-phenyl-pent-3-en-2-one-(2,4-dinitro-phenylhydrazone) 
• 15121-66-1 4-Hydroxy-4-phenyl-2-pentanone 
• 827-69-0 (E)-4-phenyl-3-penten-2-one 
• 61455-19-4 N-(1,1-Dimethyl-3,3-diphenyl-butyl)-formamide 
• 61455-12-7 Bis-(1,1-dimethyl-3,3-diphenyl-butyl)-diazene 
• 1592890-25-9 (E)-(4-methylhepta-1,5-dien-4-yl)benzene 
• 1592890-27-1 (E)-(4-methylhepta-2,6-dien-2-yl)benzene 
• 104174-53-0 4-phenyl-3-penten-2-ol 
• 4467-33-8 6-methyl-4-phenyl-2H-pyran-2-one 
• 106538-99-2 (R)-4-hydroxy-4-phenylpentan-2-one 
• 36567-70-1 (3R)-3-phenyl-3-hydroxybutanoic acid 
• 1239568-87-6 (S)-4-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pentan-2-one 

Relevant articles and documents

Lewis Acid Catalyzed Ring-Opening Reaction of Cyclobutanones towards Conjugated Enones

An unprecedented Fe-catalyzed ring-opening reaction of simple cyclobutanones is developed, which provides access to conjugated enones with good functional group tolerance in high yields under mild conditions. The product derivatization and gram-scale expe

Tuning the Reactivity of Functionalized Diallylic Alcohols: Br?nsted versus Lewis Acid Catalysis

The chemodivergent reactivity of bifunctional, enol thioether-containing diallylic alcohols in acidic medium is disclosed, highlighting the difference between strong Lewis acid and mild Br?nsted acid catalysis. In the presence of bismuth(III) triflate, allylic alcohol activation affords diversely substituted cyclopentenones in a Nazarov-type electrocyclization, whereas activation of the thioenol ether by p-toluenesulfonic acid provides an entry to α-sulfenylated β,γ-unsaturated ketones. Both methods represent a facile access to the corresponding products under mild conditions, using inexpensive and non-toxic catalytic systems.

Catalytic stereospecific allyl-allyl cross-coupling of internal allyl electrophiles with allylB(pin)

Application of internal electrophiles in catalytic stereospecific allyl-allyl cross-coupling enable the rapid construction of multisubstituted 1,5-dienes, including those with all carbon quaternary centers. Compounds with minimal steric differentiation ca