128217-58-3

Basic information

• Product Name: (3'R,4'R,5'S,6'S)-5-(2-(Benzyloxy)ethyl)-4'-benzenesulfonamidobicyclo<2.2.1>heptane
• Synonyms: (3'R,4'R,5'S,6'S)-5-(2-(Benzyloxy)ethyl)-4'-benzenesulfonamidobicyclo<2.2.1>heptane
• CAS NO: 128217-58-3
• Molecular Weight: 385.527
• Mol File: 128217-58-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3'R,4'R,5'S,6'S)-5-(2-(Benzyloxy)ethyl)-4'-benzenesulfonamidobicyclo<2.2.1>heptane(CAS DataBase Reference)
• NIST Chemistry Reference: (3'R,4'R,5'S,6'S)-5-(2-(Benzyloxy)ethyl)-4'-benzenesulfonamidobicyclo<2.2.1>heptane(128217-58-3)
• EPA Substance Registry System: (3'R,4'R,5'S,6'S)-5-(2-(Benzyloxy)ethyl)-4'-benzenesulfonamidobicyclo<2.2.1>heptane(128217-58-3)

Safety Data

• Hazardous Substances Data: 128217-58-3(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 128300-77-6 (4S)-3-(((3'R,4'R,5'S,6'S)-5'-(2-(Benzyloxy)ethyl)bicyclo<2.2.1>hepten-4'-yl)carbonyl)-4-(phenylmethyl)-2-oxazolidinone 
• 4799-68-2 3-benzyloxypropan-1-ol 
• 772-01-0 2-phenyl-1,3-dioxane 
• 128217-57-2 (1S,2S,3S,4R)-3-(2-Benzyloxy-ethyl)-bicyclo[2.2.1]hept-2-ylamine 
• 98-09-9 benzenesulfonyl chloride 
• 128217-55-0 (4S)-3-(((3'R,4'R,5'S,6'S)-5'-(2-(Benzyloxy)ethyl)bicyclo<2.2.1>heptan-4'-yl)carbonyl)-4-(phenylmethyl)-2-oxazolidinone 
• 128217-41-4 (4S)-3-((E)-5'-(Benzyloxy)-2'-penetnoyl)-4-(phenylmethyl)-2-oxazolidinone 
• 128217-56-1 (3'R,4'R,5'S,6'S)-5-(2-(Benzyloxy)ethyl)-4'-carboxybicyclo<2.2.1>heptane 
• 128217-53-8 5-benzyloxy-2(E)-pentenoic acid methyl ester 
• 128217-54-9 5-benzyloxy-2-(E)-pentenocarboxylic acid 
• 19790-60-4 3-Benzyloxypropanal 

Downstream Products

• 112966-96-8 Domitroban 
• 112916-68-4 (Z)-7-((1R,2S,3R,4S)-3-Benzenesulfonylamino-bicyclo[2.2.1]hept-2-yl)-hept-5-enoic acid 
• 128299-81-0 (3'R,4'R,5'S,6'S)-5'-(Formylmethyl)-4'-benzenesulfonamidobicyclo<2.2.1>heptane 
• 128217-59-4 (3'R,4'R,5'S,6'S)-5'-(2-Hydroxyethyl)-4'-benzenesulfonamidobicyclo<2.2.1>heptane 

Relevant articles and documents

Asymetric Diels-Alder Reactions with γ-Functionalized α,β-Unsaturated Chiral N-Acyloxazolidinones: Synthesis of (+)-S-145

An extension of the asymmetric Diels-Alder cycloaddition with chiral γ-substituted, α,β-unsaturated imides is described.The application of these results to the synthesis of the potent TxA2 receptor antagonist (+)-S-145 was successfully achieved in a practical manner.