Description
6-Bromoquinoline (CAS No. 5332-25-2) is a high-purity brominated quinoline derivative with the molecular formula C9H6BrN. This heterocyclic aromatic compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its versatile reactivity as a building block. Our product is rigorously tested to ensure ≥98% purity (HPLC/GC), with trace metal analysis available upon request. Supplied as a crystalline solid with typical lot-specific characterization data including 1H/13C NMR spectra and mass spectrometry reports. Properly packaged under inert atmosphere in amber glass vials with secure closures to ensure stability during transport and storage. Suitable for use in cross-coupling reactions (Buchwald-Hartwig, Suzuki-Miyaura), medicinal chemistry scaffold development, and coordination chemistry applications.
Properties
- CAS Number: 5332-25-2
- Complexity: 138
- IUPAC Name: 6-bromoquinoline
- InChI: InChI=1S/C9H6BrN/c10-8-3-4-9-7(6-8)2-1-5-11-9/h1-6H
- InChI Key: IFIHYLCUKYCKRH-UHFFFAOYSA-N
- Exact Mass: 206.96836
- Molecular Formula: C9H6BrN
- Molecular Weight: 208.05
- SMILES: C1=CC2=C(C=CC(=C2)Br)N=C1
- Topological: 12.9
- Monoisotopic Mass: 206.96836
- Synonyms: 6-Bromoquinoline, 5332-25-2, Quinoline, 6-bromo-, 6-bromo quinoline, KS7HD5UJ94, NSC 3996, NSC-3996, EINECS 226-238-7, DTXSID5063788, DTXCID8041400, 226-238-7, ifihylcukyckrh-uhfffaoysa-n, inchi=1/c9h6brn/c10-8-3-4-9-7(6-8)2-1-5-11-9/h1-6, 6-Bromo-quinoline, MFCD00024023, NSC3996, 6-Bromoquinoline, 97%, UNII-KS7HD5UJ94, SCHEMBL9003, CHEMBL59518, SCHEMBL208135, SCHEMBL358850, SCHEMBL944985, BCP32570, SBB001559, STK760082, AKOS005199980, AB01417, AC-3293, CCG-321550, CS-W007403, HY-W007403, PS-4259, Quinoline, 6-bromo-;6-Bromo-quinoline, ST081061, SY004614, B2015, EU-0018623, NS00032716, EN300-51894, AG-205/12083031, SR-01000523992, SR-01000523992-1, Z732220500
Application
6-Bromoquinoline serves as a key intermediate in the synthesis of quinoline-based pharmaceuticals and agrochemicals. Researchers employ this compound in palladium-catalyzed cross-coupling reactions to construct complex heterocyclic systems. The bromine substituent at the 6-position makes it particularly valuable for creating functionalized quinolines with potential biological activity. In materials science, it acts as a precursor for organic semiconductors and luminescent materials. The compound’s rigid planar structure also facilitates its use in metal-organic framework (MOF) development.
Safety and Hazards
GHS Hazard Statements
- H302 (97.7%): Harmful if swallowed [Warning Acute toxicity, oral]
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H318 (95.5%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
- H335 (97.7%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P354+P338, P317, P319, P321, P330, P332+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Acute Tox. 4 (97.7%)
- Skin Irrit. 2 (100%)
- Eye Dam. 1 (95.5%)
- STOT SE 3 (97.7%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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