75452-42-5

Basic information

• Product Name: C₃₂H₄₄O₅Si
• Synonyms: C₃₂H₄₄O₅Si
• CAS NO: 75452-42-5
• Molecular Weight: 536.784
• Mol File: 75452-42-5.mol

Chemical Properties

• CAS DataBase Reference: C₃₂H₄₄O₅Si(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₂H₄₄O₅Si(75452-42-5)
• EPA Substance Registry System: C₃₂H₄₄O₅Si(75452-42-5)

Safety Data

• Hazardous Substances Data: 75452-42-5(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 87678-99-7 1-{(2S,3R,4R,5S)-5-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3,4-dihydroxy-tetrahydro-pyran-2-yl}-propan-2-one 
• 75452-40-3 C₂₇H₃₄O₅ 
• 75452-35-6 2-(2-Benzyloxy-ethyl)-2-(2-[1,3]dioxolan-2-yl-ethyl)-malonic acid diethyl ester 
• 75452-39-0 (3S,6R)-6-Benzyloxy-3-(2-benzyloxy-ethyl)-3,6-dihydro-2H-pyran 
• 75452-37-8 2-(2-Benzyloxy-ethyl)-4-[1,3]dioxolan-2-yl-butan-1-ol 
• 75452-38-9 3-(2-benzyloxy-ethyl)-3,4-dihydro-2H-pyran 
• 75452-41-4 C₂₉H₄₀O₅Si 
• 1439-36-7 1-triphenylphosphoranylidene-2-propanone 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 32742-34-0 1,5-Anhydro-D-arabinitol 
• 87678-98-6 1-{(2S,5R)-5-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5,6-dihydro-2H-pyran-2-yl}-propan-2-one 
• 85620-85-5 3R-3,6-dihydro-2H-pyranyl-N,N-dimethylacetamide 
• 87614-56-0 5S-iodo-1S,6S-3,7-dioxabicyclo<4,3,0>nonan-8-one 

Downstream Products

• 12650-69-0 mupirocin 
• 71980-98-8 pseudomonic acid C 
• 75452-45-8 C₂₅H₄₀O₆ 
• 87678-99-7 1-{(2S,3R,4R,5S)-5-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3,4-dihydroxy-tetrahydro-pyran-2-yl}-propan-2-one 
• 87641-25-6 C₃₆H₅₀O₆Si 

Relevant articles and documents

A diastereocontrolled route to the tetrahydropyran nucleus of pseudomonic acids

A diastereocontrolled synthesis of the tetrahydropyran nucleus of pseudomonic acids has been achieved starting from a chiral building block, which we have developed. The key step is a convex-face reduction of the block having a biased framework which allo

ENANTIOSPECIFIC TOTAL SYNTHESIS OF PSEUDOMONIC ACIDS FROM ARABINOSE

The enantiospecific synthesis of pseudomonic acids from arabinose is described.