1026805-86-6

Basic information

• Product Name: (3S,4S)-[3-(4-fluoro-phenyl)-5-nitro-4-triisopropylsilanyloxymethyl-pent-1-enyl]-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
• Synonyms: (3S,4S)-[3-(4-fluoro-phenyl)-5-nitro-4-triisopropylsilanyloxymethyl-pent-1-enyl]-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
• CAS NO: 1026805-86-6
• Molecular Weight: 616.846
• Mol File: 1026805-86-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,4S)-[3-(4-fluoro-phenyl)-5-nitro-4-triisopropylsilanyloxymethyl-pent-1-enyl]-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S)-[3-(4-fluoro-phenyl)-5-nitro-4-triisopropylsilanyloxymethyl-pent-1-enyl]-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(1026805-86-6)
• EPA Substance Registry System: (3S,4S)-[3-(4-fluoro-phenyl)-5-nitro-4-triisopropylsilanyloxymethyl-pent-1-enyl]-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(1026805-86-6)

Safety Data

• Hazardous Substances Data: 1026805-86-6(Hazardous Substances Data)

Upstream product

• 111998-83-5 triisopropylsilyloxy-acetaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 53041-12-6 1-[(E)-3-bromo-1-propenyl]-4-fluorobenzene 
• 5724-03-8 1-(4-fluorophenyl)allyl alcohol 
• 329969-74-6 (E)-1-nitro-3-triisopropylsilanoxy-propene 
• 329969-73-5 [3-(4-fluoro-phenyl)-allyl]-(4-methoxy-phenyl)-carbamic acid tert-butyl ester 

Downstream Products

• 1026947-04-5 (3R,4S)-N-Boc-3-(4-fluoro-phenyl)-4-triisopropylsilanyloxymethyl-pentanol-5-amine 
• 1026071-90-8 (3R,4S)-3-(4-fluoro-phenyl)-5-nitro-4-triisopropylsilanyloxymethyl-pentanol 
• 200572-35-6 (3S,4R)-1-(tert-butoxycarbonyl)-4-(p-fluorophenyl)-3-[3,4-(methylenedioxy)phenoxymethyl]piperidine 
• 200572-34-5 (3S,4R)-tert-butyl 4-(4-fluorophenyl)-3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate 
• 200572-33-4 (3S,4R)-4-(4-fluorophenyl)-3-hydroxymethylpiperidine-1-carboxylic acid tert-butyl ester 
• 61869-08-7 paroxetine 
• 61869-08-7 paroxetine 

Relevant articles and documents

Highly diastereoselective and enantioselective carbon-carbon bond formations in conjugate additions of lithiated N-Boc allylamines to nitroalkenes: Enantioselective synthesis of 3,4- and 3,4,5-substituted piperidines including (-)-paroxetine [15]

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