445289-97-4

Basic information

• Product Name: (R)-1-((tert-butyldiphenylsilyl)oxy)pent-4-en-2-yl acrylate
• Synonyms: (R)-1-((tert-butyldiphenylsilyl)oxy)pent-4-en-2-yl acrylate
• CAS NO: 445289-97-4
• Molecular Weight: 394.586
• Mol File: 445289-97-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (R)-1-((tert-butyldiphenylsilyl)oxy)pent-4-en-2-yl acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-((tert-butyldiphenylsilyl)oxy)pent-4-en-2-yl acrylate(445289-97-4)
• EPA Substance Registry System: (R)-1-((tert-butyldiphenylsilyl)oxy)pent-4-en-2-yl acrylate(445289-97-4)

Safety Data

• Hazardous Substances Data: 445289-97-4(Hazardous Substances Data)

Upstream product

• 608130-31-0 (R)-2-(N-phenyl-aminooxy)-pent-4-en-1-ol 
• 2100-17-6 4-pentenal 
• 107033-46-5 (R)-(tert-butyldiphenylsilyloxy)methyloxirane 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 127793-64-0 (R)-1-O-(tert-butyldiphenylsilyl)-4-penten-1,2-diol 
• 814-68-6 acryloyl chloride 

Downstream Products

• 478800-46-3 6-(tert-butyl-diphenyl-silanyloxymethyl)-5,6-dihydro-2H-pyran-2-ol 
• 343981-88-4 tert-butyldiphenyl (((2R,6R)-6-isopropoxy-3,6-dihydro-2H-pyran-2-yl)methoxy)silane 
• 206651-84-5 tert-butyl(((2R)-6-isopropoxy-3,6-dihydro-2H-pyran-2-yl)-methoxy)diphenylsilane 
• 122046-63-3 (6R)-6-[(2S,3S)-3-phenyloxiran-2-yl]-5,6-dihydro-2H-pyran-2-one 
• 22639-28-7 (R)-goniothalamin 
• 64543-31-3 (-)-5R-5-hydroxydodeca-Z,Z-2,6-dienoic acid lactone 
• 206651-83-4 (R)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-5,6-dihydro-2H-pyran-2-one 

Relevant articles and documents

Stereoselective synthesis of the C1-C12 subunit of (-)-callystatin A

A stereoselective synthesis of the C1-C12 fragment of callystatin A is disclosed. The two stereocenters at C5 and C10 were created by an organocatalytic reaction and a diastereoselective alkylation, respectively. The trisubstituted double bond was introdu

An efficient synthesis of synargentolide A from D-mannitol

An efficient synthesis of synargentolide A is described by using d-mannitol and d-malic acid. The key features of the synthetic strategy include Wittig olefination, ring closing-metathesis reaction and cross-metathesis reaction for the formation of synarg

Synthesis of (R)-(-)-argentilactone

A synthesis of (R)-(-)-argentilactone is reported starting from the (S)-enantiomer of glycidol. The synthesis is based on ring closing metathesis of the acrylic ester of (R)-1-O-(tert-butyldiphenylsilyl)-4-penten-1,2-diol 4.