1342302-14-0

Basic information

• Product Name: (2S,8aS)-4-hydroxy-1-(4-methoxybenzyl)-2-propyl-1,2,6,7,8,8a-hexahydroquinoline-3-carboxylic acid allyl ester
• Synonyms: (2S,8aS)-4-hydroxy-1-(4-methoxybenzyl)-2-propyl-1,2,6,7,8,8a-hexahydroquinoline-3-carboxylic acid allyl ester
• CAS NO: 1342302-14-0
• Molecular Weight: 397.514
• Mol File: 1342302-14-0.mol

Chemical Properties

• CAS DataBase Reference: (2S,8aS)-4-hydroxy-1-(4-methoxybenzyl)-2-propyl-1,2,6,7,8,8a-hexahydroquinoline-3-carboxylic acid allyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,8aS)-4-hydroxy-1-(4-methoxybenzyl)-2-propyl-1,2,6,7,8,8a-hexahydroquinoline-3-carboxylic acid allyl ester(1342302-14-0)
• EPA Substance Registry System: (2S,8aS)-4-hydroxy-1-(4-methoxybenzyl)-2-propyl-1,2,6,7,8,8a-hexahydroquinoline-3-carboxylic acid allyl ester(1342302-14-0)

Safety Data

• Hazardous Substances Data: 1342302-14-0(Hazardous Substances Data)

Upstream product

• 225779-46-4 6-methoxycarbonyloxycyclohex-1-enecarboxylic acid methyl ester 
• 2393-23-9 4-methoxy-benzylamine 
• 1342302-07-1 3-{(6S)-6-[tert-butoxycarbonyl(4-methoxybenzyl)amino]cyclohex-1-enyl}-3-oxopropionic acid allyl ester 
• 1342302-06-0 3-{(6S)-6-[tert-butoxycarbonyl(4-methoxybenzyl)amino]cyclohex-1-enyl}-3-hydroxypropionic acid allyl ester 
• 123-72-8 butyraldehyde 
• 1342302-05-9 (1S)-(2-formylcyclohex-2-enyl)(4-methoxybenzyl)carbamic acid tert-butyl ester 
• 1342302-22-0 C₂₀H₂₉NO₄ 
• 1342302-04-8 (6S)-6-[tert-butoxycarbonyl-(4-methoxybenzyl)amino]cyclohex-1-enecarboxylic acid methyl ester 
• 932743-56-1 (6S)-6-(4-methoxybenzylamino)cyclohex-1-enecarboxylic acid methyl ester 

Downstream Products

• 1342302-08-2 (2S,8aS)-1-(4-methoxybenzyl)-2-propyl-2,3,6,7,8,8a-hexahydro-1H-quinolin-4-one 

Relevant articles and documents

Asymmetric synthesis of 2-substituted hexahydroquinolin-4-ones using a Pd-catalyzed asymmetric allylic amination and intramolecular Mannich reaction: Catalytic asymmetric synthesis of 2-epi-cis-195A

A novel method of the enantioselective synthesis of 2-substituted hexahydroquinolin-4-ones is described. The method relies on a Pd-catalyzed asymmetric allylic amination using a chiral diaminophosphine oxide (DIAPHOX) preligand and diastereoselective intr