479549-24-1

Basic information

• Product Name: 3-Cyclohexene-1,2-dicarboxylic acid, 5-[(methylsulfonyl)oxy]-, bis[(1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl] ester, (1R,2R,5R)-
• CAS NO: 479549-24-1
• Molecular Formula: C29H48O7S
• Molecular Weight: 540.762
• Mol File: 479549-24-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-Cyclohexene-1,2-dicarboxylic acid, 5-[(methylsulfonyl)oxy]-, bis[(1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl] ester, (1R,2R,5R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclohexene-1,2-dicarboxylic acid, 5-[(methylsulfonyl)oxy]-, bis[(1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl] ester, (1R,2R,5R)-(479549-24-1)
• EPA Substance Registry System: 3-Cyclohexene-1,2-dicarboxylic acid, 5-[(methylsulfonyl)oxy]-, bis[(1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl] ester, (1R,2R,5R)-(479549-24-1)

Safety Data

• Hazardous Substances Data: 479549-24-1(Hazardous Substances Data)

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 479549-21-8 (1R,2R,3Z,5R,1'S,2'R,5'S)-5-hydroxy-cyclohex-3-ene-1,2-dicarboxylic acid bis(2'-isopropyl-5'-methyl-cyclohexyl) ester 
• 15356-60-2 (1S,2R,5S)-(+)-menthol 
• 86287-64-1 (2E,1'S,2'R,5'S)-but-2-enedioic acid bis(2'-isopropyl-5'methyl-cyclohexyl) ester 
• 73627-88-0 (1R,2R,1'S,2'R,5'S)-cyclohex-4-ene-1,2-dicarboxylic acid bis(2'-isopropyl-5'-methyl-cyclohexyl) ester 
• 120143-40-0 (2Z,1'S,2'R,5'S)-but-2-enedioic acid bis(2'-isopropyl-5'methyl-cyclohexyl) ester 
• 479549-19-4 (1R,2R,4R,5R,1'S,2'R,5'S)-4-hydroxy-5-phenylselanyl-cyclohexane-1,2-dicarboxylic acid bis(2'-isopropyl-5'-methyl-cyclohexyl) ester 

Downstream Products

• 479549-29-6 (1R,2Z,6R)-cyclohex-3-ene-1,2-dicarbaldehyde 
• 479549-16-1 (1Z,3R,4R,1'E)-3,4-bis(2'-iodo-vinyl)-cyclohexene 
• 618093-66-6 C₄₄H₆₄N₂O₈Si₂ 
• 220422-37-7 epi,epi-(3''S,4''S)-polycephalin C 
• 15679-28-4 ((1R,6R)-6-(hydroxymethyl)cyclohex-3-enyl)methanol 
• 478703-63-8 (1R,2Z,6R)-(6-hydroxymethyl-cyclohex-2-enyl)methanol 

Relevant articles and documents

Total synthesis of the polyenoyltetramic acid polycephalin C

The total synthesis of the polyenoyltetramic acid polycephalin C is described. Key steps of the synthesis include a double Swern oxidation, double Takai reaction and a double Stille reaction. In addition, the absolute stereochemistry of the ring junction