ChemicalBook Product Catalog Organic Chemistry Heterocyclic Compounds 6-Bromo-1H-indole

6-Bromo-1H-indole

6-Bromo-1H-indole Basic information
Product Name:6-Bromo-1H-indole
Synonyms:EOS-60560;6-Bromoindole in stock Factory;bromoindole;BROMOINDOLE-6;6-BROMO-1H-INDOLE;6-BROMOINDOLE;6-Bromoindole,98%;bromoindole 6-Bromoindole
CAS:52415-29-9
MF:C8H6BrN
MW:196.04
EINECS:610-835-8
Product Categories:Heterocycle-Indole series;Simple Indoles;pharmacetical;Halogenated Heterocycles;Heterocyclic Building Blocks;IndolesBuilding Blocks;blocks;Bromides;IndolesOxindoles;Indole;Indoles;Heterocyclic Compounds;Halogenated;Organohalides;Indole/indoline/oxindole;Indoles and derivatives
Mol File:52415-29-9.mol
6-Bromo-1H-indole Structure
6-Bromo-1H-indole Chemical Properties
Melting point 92-96 °C (lit.)
Boiling point 70-75°C 0,01mm
density 1.660±0.06 g/cm3(Predicted)
Fp 70-75°C/0.01mm
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka16.07±0.30(Predicted)
form Powder
color White to brown
Sensitive Air & Light Sensitive
BRN 112711
InChIKeyMAWGHOPSCKCTPA-UHFFFAOYSA-N
CAS DataBase Reference52415-29-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
6-Bromo-1H-indole Usage And Synthesis
Chemical PropertiesWhite to brown powder
Uses6-Bromoindole is a starting material in the synthesis of various indole derivatives.
UsesEssential starter in 6-substituted indole chemistry.
Synthesis Reference(s)The Journal of Organic Chemistry, 49, p. 249, 1984 DOI: 10.1021/jo00176a007
General Description6-Bromoindole is an indole derivative. It undergoes palladium-catalyzed reaction with 2-(4-fluorophenyl)ethylpiperazine to afford the carbonylation products.
6-Bromo-1H-indole Preparation Products And Raw materials
Preparation Products6-Bromoindole-3-carboxaldehyde-->7-bromoquinoline-4-carboxylic acid-->AKOS B006681-->Indole-6-boronic acid-->Indole-6-boronic acid pinacol ester-->3H-Indol-3-one, 6-bromo-2-(6-bromo-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro--->Indole-->6-Bromoisatin-->3-IODO-6-BROMO INDOLE-->6-Bromo-3-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole-->1H-INDOLE-3-ACETIC ACID, 6-BROMO-α-OXO--->6-Bromo-1-(tert-butyldimethylsilyl)indole
Ethyl 6-bromoindole-2-carboxylate 1H-Indole-3-carboxylic acid, 6-bromo-1-(2-hydroxy-3-(4-morpholinyl)pro pyl)-5-methoxy-2-methyl-, ethyl ester, monohydrochloride 6-Bromo-1H-indol-4-amine 6-BROMO-DL-TRYPTOPHAN Brovincamine 6-BROMO-4-CYANOINDOLE 6-Bromoindole-3-carboxaldehyde 6-Fluoro-7-bromo-1H-indole-3-ethanol 6-BROMO-5-METHOXY-1,2-DIMETHYL-1H-INDOLE-3-CARBOXYLIC ACID 6-Bromoindole-2-carboxylic acid 2-Trimethylsilyl-7-bromo-1H-indole Brovincamine Fumarte Arbidol hydrochloride 6-BROMO-4-FLUORO-1H-INDOLE-2-CARBOXYLIC ACID (8-beta)-13-Bromo-1-(cyclopropylmethyl)-6,8-dimethylergoline Ethyl 6-bromo-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate AKOS BBS-00002569 6-Bromo-1H-indole
Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.