25177-65-5

Basic information

• Product Name: 6-(1H-INDOL-3-YL)HEXANOIC ACID
• Synonyms: Indole-3-hexanoicacid (6CI,7CI,8CI); 6-(1H-Indol-3-yl)hexanoic acid; 6-(3-Indolyl)hexanoic acid;Indole-3-caproic acid
• CAS NO: 25177-65-5
• Molecular Formula: C₁₄H₁₇NO₂
• Molecular Weight: 231.2903
• Mol File: 25177-65-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 466.5°Cat760mmHg
• Flash Point: 235.9°C
• Appearance: /
• Density: 1.184g/cm³
• Vapor Pressure: 1.68E-09mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: 6-(1H-INDOL-3-YL)HEXANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(1H-INDOL-3-YL)HEXANOIC ACID(25177-65-5)
• EPA Substance Registry System: 6-(1H-INDOL-3-YL)HEXANOIC ACID(25177-65-5)

Safety Data

• Hazardous Substances Data: 25177-65-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H17NO2/c16-14(17)9-3-1-2-6-11-10-15-13-8-5-4-7-12(11)13/h4-5,7-8,10,15H,1-3,6,9H2,(H,16,17)

Upstream product

• 502-44-3 hexahydro-2H-oxepin-2-one 
• 120-72-9 indole 

Downstream Products

• 143682-39-7 3-[6-(4-Phenyl-3,6-dihydro-2H-pyridin-1-yl)-hexyl]-1H-indole 
• 143682-27-3 6-(1H-Indol-3-yl)-1-(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)-hexan-1-one 

Relevant articles and documents

4-AMINOMETHYL-1-ARYL-CYCLOHEXYLAMINE DERIVATIVES

The invention concerns 4-aminomethyl-1-aryl-cyclohexylamine derivatives, methods for producing same, medicines containing said compounds and the use of 4-aminomethyl-1-aryl-cyclohexylamine derivatives for producing medicines.

Synthesis of 3,4-Bridged Indoles by Photocyclisation Reactions. Part 1. Photocyclisation of Halogenoacetyl Tryptophan Derivatives

Although irradiation of N-chloroacetyltryptophan results in a poor yield of photocyclisation to the indole 4-position due to competing cyclisation to C-2, the photocyclisation of (dichloroacetyl)tryptophan derivatives gives, after addition of a nucleophile in work-up, 7-substituted pyrrolobenzazocines in good yield and with trans-stereospecificity.N-(Trichloroacetyl)tryptophan derivatives also undergo photocyclisation to give 3,4-bridged indoles.The structures of the azocinoindoles 13, 21, 22 and 35, and the azepinoindole 15 were confirmed by X-ray crystallography.In one case the preparation of a cycloalkaindole was possible by the irradiation of the α-chloro amide of an indol-3-yl alkanoic acid.