153391-18-5

Basic information

• Product Name: (2S,3aS,7aS)-1-((R)-3-Phenyl-4,5-dihydro-isoxazole-5-carbonyl)-octahydro-indole-2-carboxylic acid ethyl ester
• Synonyms: (2S,3aS,7aS)-1-((R)-3-Phenyl-4,5-dihydro-isoxazole-5-carbonyl)-octahydro-indole-2-carboxylic acid ethyl ester
• CAS NO: 153391-18-5
• Molecular Weight: 370.448
• Mol File: 153391-18-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3aS,7aS)-1-((R)-3-Phenyl-4,5-dihydro-isoxazole-5-carbonyl)-octahydro-indole-2-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3aS,7aS)-1-((R)-3-Phenyl-4,5-dihydro-isoxazole-5-carbonyl)-octahydro-indole-2-carboxylic acid ethyl ester(153391-18-5)
• EPA Substance Registry System: (2S,3aS,7aS)-1-((R)-3-Phenyl-4,5-dihydro-isoxazole-5-carbonyl)-octahydro-indole-2-carboxylic acid ethyl ester(153391-18-5)

Safety Data

• Hazardous Substances Data: 153391-18-5(Hazardous Substances Data)

Upstream product

• 79815-20-6 (S)-indoline-2-carboxylic acid 
• 82923-81-7 (S)-2,3-dihydro-1H-indole-2-carboxylic acid ethyl ester 
• 89083-53-4 ethyl (2α, 3aβ, 7aβ)-octahydro-1H-indole-2-carboxylate 

Downstream Products

• 119897-89-1 (R)-3-phenyl-Δ²-isoxazoline-5-methanol 

Relevant articles and documents

Asymmetric 1,3-dipolar cycloaddition of nitrile oxides to new chiral acrylamides derived from (S)-indoline-2-carboxylic acid

Asymmetric 1,3-dipolar cycloaddition of nitrile oxides to new chiral acrylamides (3a-c) is reported to give the chiral Δ2-isoxazolines with the high diastereoselectivity (up to 95:5).