291520-37-1

Basic information

• Product Name: 1-methyl-(4S)-isopropyl-(5R)-dimethyl acetal-1-cyclohexen-6-one
• Synonyms: 1-methyl-(4S)-isopropyl-(5R)-dimethyl acetal-1-cyclohexen-6-one
• CAS NO: 291520-37-1
• Molecular Weight: 226.316
• Mol File: 291520-37-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-methyl-(4S)-isopropyl-(5R)-dimethyl acetal-1-cyclohexen-6-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-(4S)-isopropyl-(5R)-dimethyl acetal-1-cyclohexen-6-one(291520-37-1)
• EPA Substance Registry System: 1-methyl-(4S)-isopropyl-(5R)-dimethyl acetal-1-cyclohexen-6-one(291520-37-1)

Safety Data

• Hazardous Substances Data: 291520-37-1(Hazardous Substances Data)

Upstream product

• 499-71-8 carvotanacetone 
• 149-73-5 trimethyl orthoformate 
• 2244-16-8 (S)-p-mentha-6,8-dien-2-one 

Downstream Products

• 291520-45-1 ((1R,2R,6R)-2-Benzenesulfonylmethyl-6-isopropyl-3-methyl-cyclohex-3-enylmethoxy)-tert-butyl-dimethyl-silane 
• 291520-44-0 ((1R,2R,6R)-2-Benzenesulfonylmethyl-6-isopropyl-3-methyl-cyclohex-3-enyl)-methanol 
• 291520-69-9 (1R,2R,6R)-6-Isopropyl-3-methyl-2-phenylsulfanylmethyl-cyclohex-3-enecarboxylic acid methyl ester 
• 291520-42-8 (1R,2R,6R)-6-Isopropyl-3-methyl-2-phenylsulfanylmethyl-cyclohex-3-enecarboxylic acid 
• 291520-43-9 ((1R,2R,6R)-6-Isopropyl-3-methyl-2-phenylsulfanylmethyl-cyclohex-3-enyl)-methanol 
• 291520-39-3 1-methyl-(4R)-isopropyl-(5R)-dimethyl acetal-6(S)-hydroxymethyl-1-cyclohexene 
• 221290-72-8 {(2R,3R)-3-[(1R,5R,6R)-6-dimethoxymethyl-5-isopropyl-2-methyl-cyclohex-2-enylmethyl]-2-methyl-oxiranyl}-methanol 
• 221290-59-1 (E)-4-[(1R,5R,6R)-6-dimethoxymethyl-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol 
• 221290-58-0 (Z)-4-[(1R,5R,6R)-6-dimethoxymethyl-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol 
• 291520-38-2 (4R,5R)-5-Dimethoxymethyl-4-isopropyl-1-methyl-6-methylene-cyclohexene 

Relevant articles and documents

Studies on the stereoselective synthesis of the marine antitumor agent eleutherobin

(+)-Carvone has been converted into the sulfone 14 which comprises the left-hand side of the cytotoxic sesquiterpene, eleutherobin 1. Julia coupling of 14 to the aldehyde 21, followed by oxidation, dissolving metal reduction and stereoselective reduction