71054-83-6

Basic information

• Product Name: 3-Hydroxy-1-phenylmethyl-1H-indol-2-yl methyl ketone
• CAS NO: 71054-83-6
• Molecular Weight: 265.312
• Mol File: 71054-83-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Hydroxy-1-phenylmethyl-1H-indol-2-yl methyl ketone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Hydroxy-1-phenylmethyl-1H-indol-2-yl methyl ketone(71054-83-6)
• EPA Substance Registry System: 3-Hydroxy-1-phenylmethyl-1H-indol-2-yl methyl ketone(71054-83-6)

Safety Data

• Hazardous Substances Data: 71054-83-6(Hazardous Substances Data)

Upstream product

• 78-95-5 chloroacetone 
• 6622-55-5 N-benzylanthranilic acid 

Downstream Products

• 157865-20-8 1,4-Dihydro-2,6-dimethyl-4-(5-benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-2-yl)pyridin-3,5-dicarbonsaeurediethylester 
• 156418-23-4 1,4-Dihydro-2,6-dimethyl-4-(5-benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-3-yl)pyridin-3,5-dicarbonsaeurediethylester 
• 157865-11-7 1,4-Dihydro-2,6-dimethyl-4-(5-benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-2-yl)pyridin-3,5-dicarbonsaeuredimethylester 
• 156418-33-6 4,6-Dimethyl-2-(5-benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-3-yl)pyridin-3,5-dicarbonsaeuredimethylester 
• 156418-21-2 1,4-Dihydro-2,6-dimethyl-4-(5-benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-3-yl)pyridin-3,5-dicarbonsaeuredimethylester 
• 156418-29-0 2,6-Dimethyl-4-(5-benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-3-yl)pyridin-3,5-dicarbonsaeuredimethylester 
• 157865-08-2 (Z)-5-Benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-2-carbaldoxim 
• 157865-04-8 5-Benzyl-3-hydroxymethyl-pyrano<3,2-b>indol-4(5H)-on 
• 157865-09-3 5-Benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-2-carbonitril 
• 157865-05-9 5-Benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-2-carbaldehyd 
• 156418-04-1 5-Benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-3-carbaldehyd 
• 71054-86-9 5-Benzyl-4,5-dihydro-4-oxo-pyrano<3,2-b>indol-2-carbonsaeureethylester 

Relevant articles and documents

Synthesis and reactions of 4,5-dihydro-4-oxo-pyrano [3,2-b]indole-3-carbaldehydes

The title substances 3 are accessible following two reaction pathes, beginning with the 1,3-dicarbonyl compounds I. The 2-amino-3-carbaldehydes 15 are synthesized from the oximes II. The reaction of 3 with β-amino crotonic esters yields a mixture of the 1

Process for the preparation of indolopyrones

This invention relates to a novel process for preparing a group of novel substituted indolopyrones.