97579-31-2

Basic information

• Product Name: C₃₇H₅₀O₆
• Synonyms: C₃₇H₅₀O₆
• CAS NO: 97579-31-2
• Molecular Weight: 590.8
• Mol File: 97579-31-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₃₇H₅₀O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₇H₅₀O₆(97579-31-2)
• EPA Substance Registry System: C₃₇H₅₀O₆(97579-31-2)

Safety Data

• Hazardous Substances Data: 97579-31-2(Hazardous Substances Data)

Upstream product

• 628-71-7 1-Heptyne 
• 3969-59-3 mannitol triacetonide 
• 3969-84-4 3,4-di-O-isopropylidene-D-mannitol 
• 53754-41-9 1,6-di-O-(p-toluenesulfonyl)-3,4-O-isopropylidene-D-mannitol 
• 63700-05-0 1,2;5,6-dianhydro-3,4-O-isopropylidene-D-mannitol 
• 98-88-4 benzoyl chloride 
• 97579-27-6 C₃₇H₄₆O₆ 

Downstream Products

• 71160-24-2 Leukotriene B 
• 82493-55-8 6(R)-<(tert-butyldiphenylsilyl)oxy>-2(E),4(E),8(Z)-tetradecatrien-1-ol 
• 101398-98-5 1-bromo-6(R)-<(tert-butyldiphenylsilyl)oxy>-2(E),4(E),8(Z)-tetradecatriene 
• 82493-56-9 <6(R)-<(tert-butyldiphenylsilyl)oxy>-2(E),4(E),8(Z)-tetradecatrien-1-yl>triphenylphosphonium bromide 
• 97579-37-8 2(R)-(benzyloxy)dec-4(Z)-enal 
• 82498-75-7 ethyl 6(R)-<(tert-butyldiphenylsilyl)oxy>-2(E).4(E),8(Z)-tetradecatrienoate 
• 82493-59-2 ethyl 5(S)-(benzoyloxy)-12(R)-<(tert-butyldiphenylsilyl)oxy>-6(Z),8(E),10(E),14(Z)-icosatetraenoate 
• 82493-61-6 ethyl 5(S)-(benzoyloxy)-12(R)-<(tert-butyldiphenylsilyl)oxy>-6(E),8(E),10(E),14(Z)-icosatetraenoate 
• 82493-60-5 (5S,12R,6Z,8E,10E,14Z)-ethyl 5-benzoyloxy-12-hydroxyicosatetra-6,8,10,14-enoate 
• 119392-37-9 4(R)-(benzoyloxy)dodeca-2(E),6(Z)-dienal 
• 119392-38-0 ethyl 6(R)-(benzoyloxy)-2(E)-4(E),8(Z)-tetradecatrienoate 
• 119392-39-1 ethyl 6(S)-(benzoyloxy)-13(R)-<(tert-butyldiphenylsilyl)oxy>-7(Z),9(E),11(E),15(Z)-henicosatetraenoate 
• 119413-60-4 ethyl 6(S)-(benzoyloxy)-13(R)-<(tert-butyldiphenylsilyl)oxy>-7(E),9(E),11(E),15(Z)-henicosatetraenoate 
• 97579-36-7 (2R,4Z)-2-Benzoyloxydec-4-en-1-al 

Relevant articles and documents

Total Synthesis of Leukotriene B44> and Homo-LTB4 from D-Mannitol

A convergent total synthesis of leukotriene B4 and its homo analogue has been carried out via enantiomerically pure α-hydroxy aldehydes, chiral key intermediates obtained from D-mannitol and connected at a four carbon atom interval by Wittig re