506449-82-7

Basic information

• Product Name: (2S,6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2-hydroxy-2,8-dimethyl-3-oxo-decanoic acid benzyl ester
• Synonyms: (2S,6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2-hydroxy-2,8-dimethyl-3-oxo-decanoic acid benzyl ester
• CAS NO: 506449-82-7
• Molecular Weight: 492.772
• Mol File: 506449-82-7.mol

Chemical Properties

• CAS DataBase Reference: (2S,6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2-hydroxy-2,8-dimethyl-3-oxo-decanoic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2-hydroxy-2,8-dimethyl-3-oxo-decanoic acid benzyl ester(506449-82-7)
• EPA Substance Registry System: (2S,6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2-hydroxy-2,8-dimethyl-3-oxo-decanoic acid benzyl ester(506449-82-7)

Safety Data

• Hazardous Substances Data: 506449-82-7(Hazardous Substances Data)

Upstream product

• 94424-88-1 (2R,3R)-3-(ethyloxiran-2-yl)methanol 
• 345915-36-8 (2S,4S)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-4-methyl-hexan-1-ol 
• 345915-40-4 (4R,6S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-methyl-octanal 
• 506449-80-5 (E)-(6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2,8-dimethyl-dec-2-enoic acid benzyl ester 
• 506449-77-0 (2R,4S)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-4-methyl-hexanal 
• 506449-74-7 (2S,3R)-2-((S)-2-Methyl-butyl)-pentane-1,3-diol 
• 6261-22-9 pent-2-yn-1-ol 
• 1576-96-1 (E)-2-penten-1-ol 
• 506449-81-6 (2S,3R,6R,8S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-2,3-dihydroxy-2,8-dimethyl-decanoic acid benzyl ester 
• 1027310-56-0 2,2-Dimethyl-propionic acid (2S,4S)-2-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-propyl]-4-methyl-hexyl ester 
• 506449-78-1 (E)-(4S,6S)-4-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-methyl-oct-2-enoic acid ethyl ester 

Relevant articles and documents

Synthesis of the acyl side chain segment of polyoxypeptins using regioselective ring-opening of chiral 2,3-epoxy alcohol

The acyl side chain segment 2 contained in polyoxypeptins A (1a) and B (1b), apoptosis-inducing cyclodepsipeptides, was synthesized from chiral 2,3-epoxy alcohol (6), easily prepared by Sharpless asymmetric epoxidation, through a regioselective ring-opening reaction as the key step.