93292-66-1

Basic information

• Product Name: <(4S)-(2E)-4-tert-butyldiphenylsilyloxy-2-nonen-yl>triphenylphosphonium bromide
• CAS NO: 93292-66-1
• Molecular Weight: 721.833
• Mol File: 93292-66-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: <(4S)-(2E)-4-tert-butyldiphenylsilyloxy-2-nonen-yl>triphenylphosphonium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: <(4S)-(2E)-4-tert-butyldiphenylsilyloxy-2-nonen-yl>triphenylphosphonium bromide(93292-66-1)
• EPA Substance Registry System: <(4S)-(2E)-4-tert-butyldiphenylsilyloxy-2-nonen-yl>triphenylphosphonium bromide(93292-66-1)

Safety Data

• Hazardous Substances Data: 93292-66-1(Hazardous Substances Data)

Upstream product

• 118908-15-9 (E)-(S)-4-(tert-Butyl-diphenyl-silanyloxy)-non-2-enal 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 93292-41-2 2-deoxy-3-O-(tert-butyldiphenylsilyl)-4,5-O-isopropylidene-D-erythro-pentose diethyl dithioacetal 
• 93292-42-3 2-deoxy-3-O-(tert-butyldiphenylsilyl)-4,5-bis-O-(1-methylethylidene)-D-erythro-pentose 
• 93292-62-7 (2R,3S)-3-(tert-Butyl-diphenyl-silanyloxy)-octane-1,2-diol 
• 93292-61-6 tert-Butyl-[(S)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexyloxy]-diphenyl-silane 
• 133988-97-3 ethyl (4S)-(2E)-4-tert-butyldiphenylsilyloxy-2-nonenoate 
• 93292-64-9 (4S),(2E)-4-O-tert-butyldiphenylsilyloxy-2-nonenol 
• 93292-63-8 (S)-2-(tert-butyldiphenylsilyloxy)heptanal 
• 603-35-0 triphenylphosphine 
• 93292-65-0 1-bromo-(4S),(2E)-4-tert-butyldiphenylsilyloxy-2-nonene 

Downstream Products

• 94235-43-5 4-{(2S,3S)-3-[(1E,3E,5Z,7E)-(S)-9-(tert-Butyl-diphenyl-silanyloxy)-tetradeca-1,3,5,7-tetraenyl]-oxiranyl}-butyric acid ethyl ester 
• 94235-56-0 (5S,6R,15S)-(7E,9E,11Z,13E)-15-O-tert-butyldiphenylsilyl-5,6-O-carbonyllipoxin A₄ ethyl ester 
• 94292-89-4 4-{(4S,5R)-5-[(1E,3E,5E,7E)-(S)-9-(tert-Butyl-diphenyl-silanyloxy)-tetradeca-1,3,5,7-tetraenyl]-2-oxo-[1,3]dioxolan-4-yl}-butyric acid ethyl ester 

Relevant articles and documents

Lipoxins A4 and B4. Total Synthesis Including Deprotection Studies

The total synthesis of lipoxins A4 and B4 (LXA4 and LXB4) as well as of their all-trans isomers is reported.A study concerning the final steps of deprotection of silyl ether, cyclic carbonate and ethyl ester assisted by a high-speed scanning UV spectropho

The total syntheses of several 8,15 dihydroxy arachidonic acid derivatives (8,15, LTB's)

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