5515-77-5

Basic information

• Product Name: 4-ethyl-2-cyclohexen-1-one
• Synonyms: 4-ethyl-2-cyclohexen-1-one
• CAS NO: 5515-77-5
• Molecular Weight: 124.183
• Mol File: 5515-77-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-ethyl-2-cyclohexen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ethyl-2-cyclohexen-1-one(5515-77-5)
• EPA Substance Registry System: 4-ethyl-2-cyclohexen-1-one(5515-77-5)

Safety Data

• Hazardous Substances Data: 5515-77-5(Hazardous Substances Data)

Upstream product

• 274931-15-6 2-bromo-4-ethylcyclohexanone ethylene ketal 
• 1515-95-3 p-ethylanisole 
• 35650-55-6 2-ethyl-5-oxo-hexanal 
• 36881-00-2 2-(4-methoxyphenyl)-2-methyI-1,3-dioxolane 
• 5441-51-0 4-ethylcyclohexanone 
• 274931-16-7 4-ethyl-2-cyclohexenone ethylene ketal 

Downstream Products

• 274931-17-8 diethyl (4-ethylcyclohexanon-3-yl)malonate 
• 1393359-58-4 methyl 2-cyano-2-(4-ethyl-1-oxocyclohexane-3-yl)acetate 
• 123-07-9 4-Ethylphenol 
• 517-81-7 20-epiuleine 

Relevant articles and documents

Palladium-Catalyzed Ullmann Cross-Coupling/Tandem Reductive Cyclization Route to Key Members of the Uleine Alkaloid Family

The trisubstituted cyclohexenone 12, generated through a palladium-catalyzed Ullmann cross-coupling reaction between o-iodonitrobenzene and a 4,5-trans-disubstituted 2-iodo-2-cyclohexen-1-one, engaged in a tandem reductive cyclization process upon exposur

Intermediates for the synthesis of indole alkaloids. Synthesis of tetrahydrocarbazole derivatives

The synthesis of new precursors 8 and 15 for the synthesis of tetracyclic indole alkaloids were described. Many new intermediates 4-7 and 9-14 have also been synthesized.

ALKALI METAL-HEXAMETHYLPHOSPHORAMIDE REDUCTION. PART V. REDUCTION OF SOME MONO- AND DIALKYLANISOLES BY LITHIUM IN HMPA

o-, m- and p-Alkylanisoles have been reduced.To extend our observations some dialkylanisoles have been reduced, too.In most cases results comparable with those in Birch reduction have been obtained.