126503-54-6

Basic information

• Product Name: (4R,5R,6R,4'R,5'R,6'R)-4,5,4',5'-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6'-bis-(tert-butyl-dimethyl-silanyloxymethyl)-5,6,5',6'-tetrahydro-4H,4'H-[2,2']bipyranyl
• Synonyms: (4R,5R,6R,4'R,5'R,6'R)-4,5,4',5'-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6'-bis-(tert-butyl-dimethyl-silanyloxymethyl)-5,6,5',6'-tetrahydro-4H,4'H-[2,2']bipyranyl
• CAS NO: 126503-54-6
• Molecular Weight: 975.846
• Mol File: 126503-54-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4R,5R,6R,4'R,5'R,6'R)-4,5,4',5'-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6'-bis-(tert-butyl-dimethyl-silanyloxymethyl)-5,6,5',6'-tetrahydro-4H,4'H-[2,2']bipyranyl(CAS DataBase Reference)
• NIST Chemistry Reference: (4R,5R,6R,4'R,5'R,6'R)-4,5,4',5'-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6'-bis-(tert-butyl-dimethyl-silanyloxymethyl)-5,6,5',6'-tetrahydro-4H,4'H-[2,2']bipyranyl(126503-54-6)
• EPA Substance Registry System: (4R,5R,6R,4'R,5'R,6'R)-4,5,4',5'-Tetrakis-(tert-butyl-dimethyl-silanyloxy)-6,6'-bis-(tert-butyl-dimethyl-silanyloxymethyl)-5,6,5',6'-tetrahydro-4H,4'H-[2,2']bipyranyl(126503-54-6)

Safety Data

• Hazardous Substances Data: 126503-54-6(Hazardous Substances Data)

Upstream product

• 105938-00-9 (2S,3S,4S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6-tributylstannanyl-3,4-dihydro-2H-pyran 
• 586-78-7 para-nitrophenyl bromide 
• 25245-34-5 1-bromo-2,5-dimethoxybenzene 
• 31575-75-4 2-bromophenyl benzyl ether 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 623-00-7 4-bromobenzenecarbonitrile 
• 95-46-5 2-methylphenyl bromide 
• 1829-37-4 o-bromophenyl acetate 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 108-86-1 bromobenzene 
• 106-39-8 bromochlorobenzene 

Relevant articles and documents

The Preparation of C-Arylglycals. The Palladium-Catalyzed Coupling of 3,4,6-Tri-O-(tert-butyldimethylsilyl)-1-(tributylstannyl)-D-glucal and Aryl Bromides

The palladium-catalyzed couplings of the protected 1-(tributylstannyl)-D-glucal 1 and substituted aryl bromides provide the corresponding C-arylglucals 4-15 an a dimer 16 resulting from the homocoupling of 1.