101348-96-3

Basic information

• Product Name: 3-Benzyloxy-5-(imidazole-1-carbonyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester
• Synonyms: 3-Benzyloxy-5-(imidazole-1-carbonyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester
• CAS NO: 101348-96-3
• Molecular Weight: 421.453
• Mol File: 101348-96-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-Benzyloxy-5-(imidazole-1-carbonyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Benzyloxy-5-(imidazole-1-carbonyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester(101348-96-3)
• EPA Substance Registry System: 3-Benzyloxy-5-(imidazole-1-carbonyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester(101348-96-3)

Safety Data

• Hazardous Substances Data: 101348-96-3(Hazardous Substances Data)

Upstream product

• 101348-94-1 5-Benzyloxy-2-(3-ethoxycarbonyl-propyl)-pyridine-3,4-dicarboxylic acid 3-benzyl ester 4-ethyl ester 
• 101348-93-0 2-(3-(ethoxycarbonyl)propyl)-3-(ethoxycarbonyl)-4-((benzyloxy)carbonyl)-5-(benzyloxy)pyridine 
• 101349-07-9 3-Benzyloxy-5-oxo-5,6,7,8-tetrahydro-quinoline-4,6-dicarboxylic acid diethyl ester 
• 101348-92-9 2-(3-Ethoxycarbonyl-propyl)-5-hydroxy-pyridine-3,4-dicarboxylic acid 4-ethyl ester 
• 101348-95-2 3-(benzyloxy)-4-(ethoxycarbonyl)-5-oxo-5,6,7,8-tetrahydroquinoline 
• 88889-11-6 3-(benzyloxy)-4-(ethoxycarbonyl)-5,6,7,8-tetrahydro-5-hydroxyquinoline 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 101348-97-4 (S)-3-Benzyloxy-5-((S)-1-phenyl-ethylcarbamoyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester 
• 88889-12-7 (R)-3-Benzyloxy-5-((S)-1-phenyl-ethylcarbamoyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester 
• 101349-09-1 (R)-3-Benzyloxy-5-(3-dimethylamino-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-4-carbaldehyde oxime 
• 88929-66-2 (S)-3-Benzyloxy-5-hydroxy-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester 
• 101349-01-3 [3-((R)-4-Aminomethyl-3-benzyloxy-5,6,7,8-tetrahydro-quinolin-5-ylsulfanyl)-propyl]-dimethyl-amine 
• 101349-00-2 [(R)-3-Benzyloxy-5-(3-dimethylamino-propylsulfanyl)-5,6,7,8-tetrahydro-quinolin-4-yl]-methanol 
• 88889-13-8 (R)-3-Benzyloxy-5-(3-dimethylamino-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-4-carbaldehyde 
• 101348-98-5 (R)-3-Benzyloxy-5-(3-dimethylamino-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester 
• 101349-08-0 (S)-3-Benzyloxy-5-methanesulfonyloxy-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester 
• 88889-12-7 3-Benzyloxy-5-((S)-1-phenyl-ethylcarbamoyloxy)-5,6,7,8-tetrahydro-quinoline-4-carboxylic acid ethyl ester 

Relevant articles and documents

Mimics of Transaminase Enzymes

Pyridoxamine has been attached to the primary side and to the secondary side of β-cyclodextrin; the resulting compounds convert α-keto acids to amino acids with substrate selectivity and some stereoselectivity.Pyridoxamine has also been attached to a synthetic macrocycle; the attached binding group showed substrate selectivity.Chains carrying catalytic basic groups have been attached to pyridoxamine; appropriate systems catalyze the prototropic rearrangement characteristic of transamination.A catalyzed HCl elimination involving chloropyruvic acid was observed.A tetrahydroquinoline system related to pyridoxamine was synthesized to permit the stereochemically defined placement of a basis catalytic group.This converted keto acids to amino acids with good stereoselectivity for the formation of optically active products.