1174166-09-6

Basic information

• Product Name: (1R)-1-[(2R,3R)-3-phenyloxiran-2-yl]but-3-en-1-ol
• Synonyms: (1R)-1-[(2R,3R)-3-phenyloxiran-2-yl]but-3-en-1-ol
• CAS NO: 1174166-09-6
• Molecular Weight: 190.242
• Mol File: 1174166-09-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R)-1-[(2R,3R)-3-phenyloxiran-2-yl]but-3-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R)-1-[(2R,3R)-3-phenyloxiran-2-yl]but-3-en-1-ol(1174166-09-6)
• EPA Substance Registry System: (1R)-1-[(2R,3R)-3-phenyloxiran-2-yl]but-3-en-1-ol(1174166-09-6)

Safety Data

• Hazardous Substances Data: 1174166-09-6(Hazardous Substances Data)

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 79299-29-9 (E)-1-phenyl-1,5-hexadien-3-ol 
• 13891-95-7 (1E,3R)-1-phenyl-1,5-hexadien-3-ol 

Downstream Products

• 1174166-10-9 (1R)-1-[(2R,3R)-(3-phenyloxiran-2-yl)]but-3-enyl acrylate 
• 1429195-13-0 (1S,2S,3R)-1-azido-1-phenylhex-5-ene-2,3-diol 
• 1429195-14-1 C₁₆H₁₉N₃O₄ 
• 1429195-15-2 C₁₃H₁₃N₃O₃ 
• 1429195-16-3 C₂₅H₃₇N₃O₂ 
• 1429195-17-4 C₂₇H₄₅NO₃ 
• 1429195-18-5 C₂₆H₂₇N₃O₂ 
• 1429195-19-6 C₃₇H₄₉N₃O₂ 

Relevant articles and documents

A stereocontrolled route to d-ribo-phytosphingosine and sphinganine from an achiral secondary homoallylic alcohol using Sharpless kinetic resolution

A facile and efficient enantioselective route for the synthesis of d-ribo-phytosphingosine (1a) and sphinganine (1b) has been developed employing commercially available and cheap starting material trans-cinnamaldehyde 2. The synthetic strategy features the Sharpless kinetic resolution, regioselective epoxide opening and Wittig olefination as the key steps.