124267-38-5

Basic information

• Product Name: 2-methyl-3-propenyl-2-cyclohexenone
• Synonyms: 2-methyl-3-propenyl-2-cyclohexenone
• CAS NO: 124267-38-5
• Molecular Weight: 150.221
• Mol File: 124267-38-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-methyl-3-propenyl-2-cyclohexenone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-3-propenyl-2-cyclohexenone(124267-38-5)
• EPA Substance Registry System: 2-methyl-3-propenyl-2-cyclohexenone(124267-38-5)

Safety Data

• Hazardous Substances Data: 124267-38-5(Hazardous Substances Data)

Upstream product

• 150765-78-9 2-methyl-3-oxocyclohex-1-en-1-yl trifluoromethanesulfonate 
• 83947-58-4 4,4,5,5-tetramethyl-2-[(1E)-prop-1-en-1-yl]-1,3,2-dioxaborolane 
• 37457-15-1 3-isobutoxy-2-methyl-2-cyclohexen-1-one 
• 89998-56-1 3-ethynyl-2-methylcyclohex-2-en-1-one 
• 61765-56-8 3-cyclopropyl-2-methyl-2-cyclohexen-1-one 
• 56671-84-2 3-iodo-2-methylcyclohexenone 

Relevant articles and documents

Ru-catalyzed isomerization of ω-alkenylboronates towards stereoselective synthesis of vinylboronates with subsequent: In situ functionalization

The stereoselective preparation of synthetically versatile vinylboronates from ω-alkenylboronates is achieved through a ruthenium-catalyzed isomerization reaction. A variety of di- A nd trisubstituted vinylboronates were conveniently produced and could be

Five-membered ring annulation via thermal rearrangement of β-cyclopropyl α,β-unsaturated ketones. A formal total synthesis of the sesquiterpenoid (+/-)-zizaene

Treatment of the β-iodo enones 7-10 with lithium(phenylthio)cyclopropyl cuprate provided excellent yields of the corresponding β-cyclopropyl α,β-unsaturated ketones 11-14, respectively.When 3-isopropenyl-2-cyclohexen-1-one (16) was allowed to react with d