151153-99-0

Basic information

• Product Name: 2-Oxazolidinone, 3-[(4-methyl-3-cyclohexen-1-yl)carbonyl]-
• CAS NO: 151153-99-0
• Molecular Formula: C11H15NO3
• Molecular Weight: 209.245
• Mol File: 151153-99-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Oxazolidinone, 3-[(4-methyl-3-cyclohexen-1-yl)carbonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone, 3-[(4-methyl-3-cyclohexen-1-yl)carbonyl]-(151153-99-0)
• EPA Substance Registry System: 2-Oxazolidinone, 3-[(4-methyl-3-cyclohexen-1-yl)carbonyl]-(151153-99-0)

Safety Data

• Hazardous Substances Data: 151153-99-0(Hazardous Substances Data)

Upstream product

• 2043-21-2 acryloyl-1,3-oxazolidin-2-one 
• 78-79-5 isoprene 

Downstream Products

• 4342-60-3 4-methylcyclohex-3-enecarboxylic acid 
• 90719-40-7 (4S,1'R)-3-[(4'-methylcyclohex-3'-ene-1'-yl)carbonyl]-4-iso-propyloxazolidin-2-one 
• 16695-95-7 (4'-methylcyclohex-3'-ene-1-'-yl)carbonyl chloride 
• 6493-79-4 methyl 4-methyl-3-cyclohexene-1-carboxylate 

Relevant articles and documents

[AlCl3 + 2THF]: A new and efficient catalytic system for Diels-Alder cycloaddition of α,β-unsaturated carbonyl compounds under solvent-free conditions

[AlCl3 + 2THF] is a new catalytic system for the Diels-Alder cycloaddition under SFC and air atmosphere. By using equimolar amounts of reactants, this catalyst prevents the polymerization of the diene and allows the corresponding adducts to be isolated with high regio- and stereocontrol and in excellent yields.

Scandium(III) triflate/isopropyl-pybox complex as an efficient catalyst for asymmetric Diels-Alder reaction

The chiral scandium (III) triflate/i-Pr-pybox complex efficiently catalyzes the asymmetric Diels-Alder reaction of 1,3-dienes with acyl-1,3-oxazolidin-2-ones (1a-c) afford the corresponding adducts in good yields with up to 90% ee. The reaction can be car

Scandium trifluoromethanesulfonate (Sc(OTf)3). A novel reusable catalyst in the Diels-Alder reaction

Scandium trifluoromethanesulfonate (Sc(OTf)3) is found to be quite effective as a Lewis acid catalyst in the Diels-Alder reaction. The novel catalyst is available in both aqueous and organic media, is easily recovered from aqueous layer after the reaction is completed, and can be reused.