116733-43-8

Basic information

• Product Name: (1R,6R)-6-(2-oxo-oxazolidine-3-carbonyl)-cyclohex-3-ene carboxylic acid methyl ester
• Synonyms: (1R,6R)-6-(2-oxo-oxazolidine-3-carbonyl)-cyclohex-3-ene carboxylic acid methyl ester
• CAS NO: 116733-43-8
• Molecular Weight: 253.255
• Mol File: 116733-43-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R,6R)-6-(2-oxo-oxazolidine-3-carbonyl)-cyclohex-3-ene carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,6R)-6-(2-oxo-oxazolidine-3-carbonyl)-cyclohex-3-ene carboxylic acid methyl ester(116733-43-8)
• EPA Substance Registry System: (1R,6R)-6-(2-oxo-oxazolidine-3-carbonyl)-cyclohex-3-ene carboxylic acid methyl ester(116733-43-8)

Safety Data

• Hazardous Substances Data: 116733-43-8(Hazardous Substances Data)

Upstream product

• 116733-42-7 3-[(E)-3-(methoxycarbonyl)-propenoyl]-oxazolidin-2-one 
• 106-99-0 buta-1,3-diene 

Downstream Products

• 323196-39-0 (1R,6R)-6-tert-butoxycarbonylamino-cyclohex-3-ene carboxylic acid methyl ester 
• 323196-40-3 (1R,6R)-6-tert-butoxycarbonylamino-cyclohex-3-ene carboxylic acid 
• 423760-35-4 (1R,2R)-2-Methanesulfonylamino-cyclohexanecarboxylic acid [(S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-amide 
• 423760-37-6 (1R,2R)-2-Methanesulfonylamino-cyclohexanecarbothioic acid [(S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-amide 
• 423760-31-0 (1R,2R)-2-Methanesulfonylamino-cyclohexanecarboxylic acid ((S)-1-hydroxymethyl-2-methyl-propyl)-amide 
• 423760-29-6 (1R,2R)-2-methanesulfonylaminocyclohexanecarboxylic acid 
• 91280-45-4 (1R,6R)-6-benzyloxycarbonylaminocyclohex-3-enecarboxylic acid methyl ester 
• 267230-45-5 (1R,2R)-2-aminocyclohexanecarboxylic acid methyl ester 
• 253454-00-1 (1S,2S)-Cyclohex-4-ene-1,2-dicarboxylic acid monomethyl ester 
• 323196-38-9 (1R,2R)-cyclohex-4-ene 1,2-dicarboxylic acid monomethyl ester 

Relevant articles and documents

Asymmetric Diels-Alder Reaction by the Use of a Chiral Titanium Catalyst with Molecular Sieves 4A. Remarkable Solvent Effect on the Enantioselectivity

A remarkable effect of solvent on the enantioselectivity was observed in the asymmetric Diels-Alder reaction of 3-(2-alkenoyl)-1,3-oxazolidin-2-ones and dienes catalyzed by a chiral titanium reagent, and the Diels-Alder adducts were obtained in high enant