907997-09-5

Basic information

• Product Name: 2-phenyl-1,4-pentadien-3-one
• Synonyms: 2-phenyl-1,4-pentadien-3-one
• CAS NO: 907997-09-5
• Molecular Weight: 158.2
• Mol File: 907997-09-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-phenyl-1,4-pentadien-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-1,4-pentadien-3-one(907997-09-5)
• EPA Substance Registry System: 2-phenyl-1,4-pentadien-3-one(907997-09-5)

Safety Data

• Hazardous Substances Data: 907997-09-5(Hazardous Substances Data)

Upstream product

• 98-81-7 1-bromovinylbenzene 
• 55177-38-3 1-[(1E)-1-methyl-1,3-butadienyl]benzene 
• 20047-25-0 4-Phenyl-(E)-3-penten-1-ol 
• 76886-55-0 Acetophenone 2,4,6-triisopropylbenzenesulphonyl hydrazone 
• 98-86-2 acetophenone 
• 907997-19-7 2-phenyl-1,4-pentadien-3-ol 

Downstream Products

• 1215036-17-1 rac-1-benzyl-4-(hydroxyimino)-3-phenylpiperidine 
• 446302-83-6 1-N-benzyl-3-phenyl-4-piperidone 

Relevant articles and documents

Synthesis of 3-aryl-substituted tetrahydropyran-4-ones and tetrahydrothiopyran-4-ones

A series of tetrahydropyran-4-one and tetrahydrothiopyran-4-one derivatives with 3-aryl or 3,6-diaryl substituents were prepared by double conjugate addition of water or H2S to divinyl ketones. These starting materials were accessed in two step

Development of κ opioid receptor agonists by focusing on phenyl substituents of 4-dimethylamino-3-phenylpiperidine derivatives: Structure-activity relationship study of matrine type alkaloids

A series of new κ opioid receptor (KOR) agonists were developed from the lead compound 4-dimethylamino-1-pentanoylpiperidine (3), a matrine-type alkaloid. Derivatives of 3 were synthesized with a variety of phenyl substituents and evaluated for their anti

Synthesis of tetrahydropyran-4-ones and thiopyran-4-ones from donor-substituted α-bromostyrene derivatives

Tetrahydropyran-4-one and tetrahydrothiopyran-4-one derivatives with a 3-aryl substituent were synthesized by double-conjugate addition of water or H2S to divinyl ketones. These starting materials were prepared in two steps by conversion of lit