223558-55-2

Basic information

• Product Name: (2R,3S)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol
• Synonyms: (2R,3S)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol
• CAS NO: 223558-55-2
• Molecular Weight: 396.602
• Mol File: 223558-55-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,3S)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol(223558-55-2)
• EPA Substance Registry System: (2R,3S)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol(223558-55-2)

Safety Data

• Hazardous Substances Data: 223558-55-2(Hazardous Substances Data)

Upstream product

• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 212579-64-1 (4R)-1-(2,2-dimethyl-[1,3]dioxolan-4-yl)allyl alcohol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 18524-19-1 (S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-prop-2-en-1-ol 

Downstream Products

• 209479-87-8 tert-Butyl-((S)-3,3-dibromo-1-vinyl-allyloxy)-diphenyl-silane 
• 18524-19-1 (S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-prop-2-en-1-ol 
• 223558-75-6 tert-Butyl-diphenyl-((Z)-(S)-1-vinyl-pentadec-7-ene-2,4-diynyloxy)-silane 
• 209479-88-9 tert-butyl((S)-1-penten-4-yn-3-yloxy)diphenylsilane 
• 81203-57-8 (3S,9Z)-1,9-heptadecadiene-4,6-diyn-3-ol 
• 334784-69-9 (2R,3S)-3-O-tert-butyldiphenylsilyl-4-pentene-1,2,3-triol 

Relevant articles and documents

Stereoselective synthesis of (3S,8R,9R,10R)-heptadeca-1-ene-4,6-diyne tetrol and its 3-epimer from D-mannitol

(3S,8R,9R,10R)-Heptadeca-1-ene-4,6-diyne tetrol and its 3-epimer were synthesized, and it was found that the relative configuration which was proposed for 1 was incorrect. Georg Thieme Verlag Stuttgart.

Absolute configuration of falcarinol, a potent antitumor agent commonly occurring in plants

The absolute configuration of falcarinol (1) was established by stereoselective total synthesis of the two enantiomers.