1353023-68-3

Basic information

• Product Name: (R)-all-trans-3-(tert-butyldimethylsilyloxy)retinal
• Synonyms: (R)-all-trans-3-(tert-butyldimethylsilyloxy)retinal
• CAS NO: 1353023-68-3
• Molecular Weight: 414.704
• Mol File: 1353023-68-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-all-trans-3-(tert-butyldimethylsilyloxy)retinal(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-all-trans-3-(tert-butyldimethylsilyloxy)retinal(1353023-68-3)
• EPA Substance Registry System: (R)-all-trans-3-(tert-butyldimethylsilyloxy)retinal(1353023-68-3)

Safety Data

• Hazardous Substances Data: 1353023-68-3(Hazardous Substances Data)

Upstream product

• 875797-48-1 (-)-(R)-all-trans-3-(tert-butyldimethylsilyloxy)retinol 

Downstream Products

• 1353023-75-2 zeaxanthin t-butyldimethylsilylether 
• 144-68-3 zeaxanthin 
• 1353023-73-0 tert-butyl-{4-[(1E,3E,5E,7E)-3,7-dimethyldeca-1,3,5,7,9-pentaenyl]-3,5,5-trimethylcyclohex-3-enyloxy}dimethylsilane 

Relevant articles and documents

Synthesis of C40-symmetrical fully conjugated carotenoids by olefin metathesis

In an effort to push olefin metathesis to the limits of conjugation in reactants and products, the C40-symmetrical carotenoids β,β-carotene (1), lycopene (2), (3R,3′R)-zeaxanthin (3), and rac-isozeaxanthin (4), which are conjugated undecaenes, have been synthesized from C21-terminal hexaenes by treatment with Grubbs' second-generation Ru catalyst in dichloromethane at 50 °C.