≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Essential starter in 6-substituted indole chemistry.
Product description：
6-Bromoindole may be used to synthesize:
6-alkylthioindole
3-acetoxy-6-bromoindole
6,6′-dibromoindigo (Tyrian purple)
6-acylindoles
tert-butyl 6-bromoindole-1-carboxylate
Essential starter in 6-substituted indole chemistry.
Application：
6-Bromoindole is an indole derivative. It undergoes palladium-catalyzed reaction with 2-(4-fluorophenyl)ethylpiperazine to afford the carbonylation products.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Indoles and derivatives |
| Subclass | Indoles |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indoles |
| Alternative Parents | Benzenoids Aryl bromides Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organobromides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Indole - Benzenoid - Aryl halide - Aryl bromide - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Organobromide - Organohalogen compound - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 J2330211 | Certificate of Analysis | Aug 04, 2026 | B123498 |
| J2330212 | Certificate of Analysis | Aug 04, 2026 | B123498 |
| J2330213 | Certificate of Analysis | Aug 04, 2026 | B123498 |
| K1702030 | Certificate of Analysis | Mar 20, 2026 | B123498 |
| J2127115 | Certificate of Analysis | Aug 12, 2024 | B123498 |
| J2127116 | Certificate of Analysis | Aug 12, 2024 | B123498 |
| A2607185 | Certificate of Analysis | Jul 01, 2024 | B123498 |
| A2607187 | Certificate of Analysis | Jul 01, 2024 | B123498 |
| I1419060 | Certificate of Analysis | Apr 02, 2024 | B123498 |
| F1424044 | Certificate of Analysis | Jan 08, 2024 | B123498 |
| Sensibilidad | light & air sensitive |
|---|---|
| Punto de ebullición (°C) | 70-75°C/0.01mm |
| Punto de fusión (°C) | 93.0-96.0°C |
| Peso molecular | 196.040 g/mol |
| XLogP3 | 3.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 194.968 Da |
| Monoisotopic Mass | 194.968 Da |
| Topological Polar Surface Area | 15.800 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 126.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
