76686-26-5

Basic information

• Product Name: [(R)-4-(1-Methoxy-1-methyl-ethoxy)-2,6,6-trimethyl-cyclohex-1-enyl]-methanol
• Synonyms: [(R)-4-(1-Methoxy-1-methyl-ethoxy)-2,6,6-trimethyl-cyclohex-1-enyl]-methanol
• CAS NO: 76686-26-5
• Molecular Weight: 242.359
• Mol File: 76686-26-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [(R)-4-(1-Methoxy-1-methyl-ethoxy)-2,6,6-trimethyl-cyclohex-1-enyl]-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [(R)-4-(1-Methoxy-1-methyl-ethoxy)-2,6,6-trimethyl-cyclohex-1-enyl]-methanol(76686-26-5)
• EPA Substance Registry System: [(R)-4-(1-Methoxy-1-methyl-ethoxy)-2,6,6-trimethyl-cyclohex-1-enyl]-methanol(76686-26-5)

Safety Data

• Hazardous Substances Data: 76686-26-5(Hazardous Substances Data)

Downstream Products

• 76686-28-7 (4R)-4-(β-D-Glucopyranosyloxy)-2,6,6-trimethyl-1-cyclohexen-1-methanol-pentaacetat 
• 76686-29-8 (4R)-4-(β-D-Glucopyranosyloxy)-2,6,6-trimethyl-1-cyclohexen-1-methanol 
• 138-55-6 (R)-4-(β-D-glucopyranosyl)-2,6,6-trimethyl-1-cyclohexene-1-carboxaldehyde 
• 42926-75-0 (4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexene-1-carbaldehyde 
• 76686-20-9 (4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexene-1-methanol 
• 76686-27-6 (3R)-3-Hydroxy-β-cyclogeranylacetat 

Relevant articles and documents

154. Synthese von optisch aktiven, natuerlichen Carotinoiden und strukturell verwandten Naturprodukten. V. Synthese von (3R,3'R)-, (3S,3'S)- und (3R,3'S; meso)-Zeaxanthin durch asymmetrische Hydroborierung. Ein neuer Zugang zu optisch aktiven Carotinoidba

The synthesis of (3R,3'R)-, (3S,3'S)- and (3R,3'S; meso)-zeaxanthin (1), (19) and (21) is reported utilizing asymmetric hydroboration as the key reaction.Thus, safranol isopropenylmethylether (4) is hydroborated with (+)- and (-)-(IPC)2BH to give the opti