395089-72-2

Basic information

• Product Name: 2,4-Hexadienal, 6-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-3-methyl-6-oxo-, (2E,4E)-
• CAS NO: 395089-72-2
• Molecular Formula: C15H22O3
• Molecular Weight: 250.338
• Mol File: 395089-72-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,4-Hexadienal, 6-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-3-methyl-6-oxo-, (2E,4E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Hexadienal, 6-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-3-methyl-6-oxo-, (2E,4E)-(395089-72-2)
• EPA Substance Registry System: 2,4-Hexadienal, 6-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-3-methyl-6-oxo-, (2E,4E)-(395089-72-2)

Safety Data

• Hazardous Substances Data: 395089-72-2(Hazardous Substances Data)

Upstream product

• 395089-70-0 (2E,4E)-5-[(1S,4S,6R)-4-(tert-Butyl-dimethyl-silanyloxy)-2,2,6-trimethyl-7-oxa-bicyclo[4.1.0]hept-1-yl]-3-methyl-penta-2,4-dienoic acid ethyl ester 
• 395089-69-7 ethyl (2E,4E)-5-[(4R)-4-tert-butyldimethylsilyloxy-2,6,6-trimethylcyclohexyl-1-enyl]-3-methylpenta-2,4-dienoate 
• 395089-71-1 (2E,4E)-3-methyl-5-[(1S,4S,6R)-4-tert-butyldimethylsilyloxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl]penta-2,4-dienal 
• 395089-68-6 ethyl (2E,4E)-5-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexyl-1-enyl]-3-methylpenta-2,4-dienoate 
• 118829-40-6 (R)-4-ethynyl-3,5,5-trimethylcyclohex-3-en-1-ol 
• 28874-44-4 (1'S,2'R,4'S,2E,4E)-5-(1',2'-Epoxy-4'-hydroxy-2',6',6'-trimethylcyclohexyl)-3-methyl-2,4-pentadienal 
• 1027513-29-6 (2E,4E)-6-[(1R,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-1,2,2-trimethyl-cyclopentyl]-3-methyl-6-oxo-hexa-2,4-dienal 

Downstream Products

• 465-42-9 capsanthin 

Relevant articles and documents

Total synthesis of cucurbitaxanthin A, cycloviolaxanthin and capsanthin 3,6-epoxide by applying a regioselective ring opening of tetrasubstituted epoxides

The synthesis of 3,6-epoxy carotenoids cucurbitaxanthin A 1, cycloviolaxanthin 2 and capsanthin 3,6-epoxide 3, was accomplished via the C15-3,6-epoxides 20e and 20f, prepared by the regioselective ring opening of the 3-hydroxy-5,6-epoxides 10e

First total synthesis of cucurbitaxanthin A applying regioselective ring opening of tetrasubstituted epoxides

The synthesis of cucurbitaxanthin A 1 was accomplished via the C 15-3,6-epoxides 7e and 7f prepared by regioselective ring opening of the 3-hydroxy-5,6-epoxides 6e and 6f.