497945-84-3

Basic information

• Product Name: 6-benzyl-8-ethoxycarbonylmethyl-3-formyl-1-methyl-1,6,7,8-tetrahydro-9-oxa-1,6-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester
• Synonyms: 6-benzyl-8-ethoxycarbonylmethyl-3-formyl-1-methyl-1,6,7,8-tetrahydro-9-oxa-1,6-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester
• CAS NO: 497945-84-3
• Molecular Weight: 464.518
• Mol File: 497945-84-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-benzyl-8-ethoxycarbonylmethyl-3-formyl-1-methyl-1,6,7,8-tetrahydro-9-oxa-1,6-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 6-benzyl-8-ethoxycarbonylmethyl-3-formyl-1-methyl-1,6,7,8-tetrahydro-9-oxa-1,6-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester(497945-84-3)
• EPA Substance Registry System: 6-benzyl-8-ethoxycarbonylmethyl-3-formyl-1-methyl-1,6,7,8-tetrahydro-9-oxa-1,6-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester(497945-84-3)

Safety Data

• Hazardous Substances Data: 497945-84-3(Hazardous Substances Data)

Upstream product

• 3724-43-4 Vilsmeier reagent 
• 462117-35-7 ethyl 4-benzyl-2-[(ethoxycarbonyl)methyl]-9-methyl-2,3,4,9-tetrahydro[1,4]oxazino[3,2-g]indole-8-carboxylate 
• 4885-02-3 Dichloromethyl methyl ether 

Downstream Products

• 497945-93-4 6-benzyl-8-ethoxycarbonylmethyl-1-methyl-3-(2-nitro-ethyl)-1,6,7,8-tetrahydro-9-oxa-1,6-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester 
• 497945-94-5 (4-benzyl-11-methyl-10-oxo-2,3,4,7,8,9,10,11-octahydro-1-oxa-4,9,11-triaza-benzo[a]fluoren-2-yl)-acetic acid ethyl ester 
• 497945-92-3 6-benzyl-8-ethoxycarbonylmethyl-1-methyl-3-(2-nitro-vinyl)-1,6,7,8-tetrahydro-9-oxa-1,6-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester 

Relevant articles and documents

A synthetic route to hexahydro[1,4]oxazino[2,3-h] and [3,2-j]β-carboline derivatives

Convenient methods for the regioselective formylation of tetrahydro[1,4]oxazino[2,3-f] and [3,2-g]indole derivatives 3 and 4 are described. The obtained formyl derivatives 6 and 8 were further transformed in four steps into the unknown hexahydro[1,4]oxazino[2,3-h] 1 and [3,2-j]β-carbolines 2.