103303-19-1

Basic information

• Product Name: (3S,4S,5S)-1-(tert-Butyl-diphenyl-silanyloxy)-3,5-dimethyl-7-trityloxy-heptan-4-ol
• CAS NO: 103303-19-1
• Molecular Weight: 656.981
• Mol File: 103303-19-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,4S,5S)-1-(tert-Butyl-diphenyl-silanyloxy)-3,5-dimethyl-7-trityloxy-heptan-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S,5S)-1-(tert-Butyl-diphenyl-silanyloxy)-3,5-dimethyl-7-trityloxy-heptan-4-ol(103303-19-1)
• EPA Substance Registry System: (3S,4S,5S)-1-(tert-Butyl-diphenyl-silanyloxy)-3,5-dimethyl-7-trityloxy-heptan-4-ol(103303-19-1)

Safety Data

• Hazardous Substances Data: 103303-19-1(Hazardous Substances Data)

Upstream product

• 103233-15-4 (2R,3S)-1-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-5-trityloxy-pentan-2-ol 
• 103246-24-8 (S)-5-((S)-1-Methyl-3-trityloxy-propyl)-3-phenylsulfanyl-dihydro-furan-2-one 
• 115479-81-7 (4S,5R)-4-Methyl-5-((S)-1-methyl-3-trityloxy-propyl)-dihydro-furan-2-one 
• 103233-14-3 (4S,5S)-5-({[tert-butyl(diphenyl)silyl]oxy}methyl)-4-methyldihydrofuran-2(3H)-one 
• 103233-16-5 4,5-anhydro-2,3-dideoxy-3-C-methyl-1-O-triphenylmethyl-D-threo-pentitol 
• 112031-78-4 (3S,4R)-5-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-pentane-1,4-diol 
• 99315-76-1 (5S)-5-(tert-butyldiphenylsiloxymethyl)-2(5H)-furanone 
• 115479-79-3 (3S,4R,5S)-3,5-Dimethyl-7-trityloxy-heptane-1,4-diol 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 103233-23-4 (3R,5R)-3,5-di-C-methyl-1-O-tert-butyldiphenylsilyl-7-O-triphenylmethyl-heptane 1,7-diol 
• 115479-80-6 Methanesulfonic acid (1S,2S)-1-[(S)-3-(tert-butyl-diphenyl-silanyloxy)-1-methyl-propyl]-2-methyl-4-trityloxy-butyl ester 

Relevant articles and documents

A Tactically Novel Alternative to Acyclic Stereoselection Based on the Concept of a Replicating Chiron - 1,3- and 1,4-C-Methyl Substitution

A chiral 4-hydroxymethyl butenolide is used as a template for the stereocontrolled conjugate addition of a C-methyl group.A sequential two-carbon extension and reformation of a lactone with the new side-chain leads to a "replicated" butenolide, which is s