21865-50-9

Basic information

• Product Name: 6-bromo-2,3,4,9-tetrahydro-1H-carbazole
• Synonyms: 6-bromo-2,3,4,9-tetrahydro-1H-carbazole;2-broMo-5,6,7,8,9,10-hexahydrocyclohepta[b]indole;6-BROMO-1,2,3,4-TETRAHYDROCARBAZOLE
• CAS NO: 21865-50-9
• Molecular Formula: C₁₂H₁₂BrN
• Molecular Weight: 250.15
• Mol File: 21865-50-9.mol
• Article Data: 26

Chemical Properties

• Melting Point: 151.5-152.0 °C
• Boiling Point: 378.7 °C at 760 mmHg
• Flash Point: 182.8 °C
• Appearance: /
• Density: 1.516 g/cm³
• Vapor Pressure: 1.34E-05mmHg at 25°C
• Refractive Index: 1.689
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 16.88±0.20(Predicted)
• CAS DataBase Reference: 6-bromo-2,3,4,9-tetrahydro-1H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 6-bromo-2,3,4,9-tetrahydro-1H-carbazole(21865-50-9)
• EPA Substance Registry System: 6-bromo-2,3,4,9-tetrahydro-1H-carbazole(21865-50-9)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 21865-50-9(Hazardous Substances Data)

Usage

General Description

6-bromo-2,3,4,9-tetrahydro-1H-carbazole is a chemical compound with the molecular formula C12H12BrN. It is a brominated derivative of tetrahydrocarbazole, a compound commonly found in plants and animals. This particular compound is used in the pharmaceutical industry for its potential applications in the development of new drugs. Its chemical structure and properties make it suitable for various medicinal purposes, including as a potential treatment for neurological disorders and as a building block in the synthesis of other biologically active compounds. Its unique structure and potential pharmaceutical uses make 6-bromo-2,3,4,9-tetrahydro-1H-carbazole an important target for further research and development.

InChI:InChI=1/C12H12BrN/c13-8-5-6-12-10(7-8)9-3-1-2-4-11(9)14-12/h5-7,14H,1-4H2

Upstream product

• 100116-02-7 2-(4-bromo-anilino)-cyclohexanone 
• 106-40-1 4-bromo-aniline 
• 117489-28-8 1-(4-bromophenyl)-2-cyclohexylidenehydrazine 
• 108-94-1 cyclohexanone 
• 589-21-9 (4-bromophenyl)hydrazine 
• 622-88-8 4-bromophenylhydrazine hydrochloride 
• 108-85-0 1-bromocyclohexane 
• 673-40-5 4-bromobenzenediazonium tetrafluoroborate 
• 41931-18-4 (4-bromophenyl)hydrazine hydrochloride salt 
• 92644-16-1 tert-butyl 2-(p-bromophenyl)hydrazine-1-carboxylate 
• 110-52-1 1,4-dibromo-butane 
• 10075-50-0 5-bromo-1H-indole 
• 1601-98-5 1,2-bis(4-bromophenyl)diazene 
• 1215-42-5 1,2-bis(4-bromophenyl)diazene oxide 

Downstream Products

• 1592-95-6 3-bromo-9H-carbazole 
• 859805-93-9 (+/-)-6-bromo-(4ar,9ac)-1,2,3,4,4a,9a-hexahydro-carbazole 
• 18992-85-3 3-methoxycarbazole 
• 1181975-27-8 6-bromo-9-(3-(3,5-dimethylphenoxy)propyl)-2,3,4,9-tetrahydro-1H-carbazole 
• 1181975-28-9 6-bromo-9-(3-(3,5-difluorophenoxy)propyl)-2,3,4,9-tetrahydro-1H-carbazole 
• 1313809-59-4 6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole 
• 1313809-70-9 6-bromo-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole 
• 1423039-46-6 4a-allyl-6-phenyl-2,3,4,4a-tetrahydro-1H-carbazole 
• 1423039-49-9 4a-allyl-6-(4-(trifluoromethyl)phenyl)-2,3,4,4a-tetrahydro-1H-carbazole 
• 1423039-50-2 4a-allyl-6-(2-fluorophenyl)-2,3,4,4a-tetrahydro-1H-carbazole 
• 1423039-52-4 4a-allyl-6-(2,6-dimethylphenyl)-2,3,4,4a-tetrahydro-1H-carbazole 
• 1423039-54-6 3-(4a-allyl-2,3,4,4a-tetrahydro-1H-carbazol-6-yl)benzonitrile 
• 893409-97-7 4-(6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-ylamino)benzonitrile 
• 59514-18-0 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-one 

Relevant articles and documents

Traceless Fischer indole synthesis on the solid phase

The Fischer indole synthesis using polymer-bound hydrazines is employed as the key step for the development of a traceless indole synthesis on a solid support.

Tetrahydrocarbazoles by mechanochemical Fischer indolisation

The Fischer indolisation (FI) typically proceeds in the presence of a Br?nsted or Lewis acid in an organic solvent at elevated temperatures. Herein, we report that tetrahydrocarbazoles (THCs) are accessible by mechanochemical FI at ambient temperature. Using phenylhydrazine hydrochlorides in the presence of silica is critical for this solid-state variant of the FI.

An electroluminescent compound and an electroluminescent device comprising the same

The present invention relates to an organic light-emitting compound represented by [Chemical formula 1]. An organic electroluminescent device comprising the organic light-emitting compound in the present invention has excellent power efficiency, light-emitting efficiency, and long life cycle because the present invention can be operated by a lower driving-voltage in comparison with a device comprising conventional phosphorescent host materials. [Chemical formula 1].