Description
3-Bromopyridine-2-carboxylic Acid (CAS No. 30683-23-9) is a high-purity, heterocyclic organic compound with the molecular formula C6H4BrNO2. This white to off-white crystalline powder is a versatile building block in pharmaceutical, agrochemical, and material science research. With a molecular weight of 202.01 g/mol, it offers excellent reactivity for coupling reactions, metal-catalyzed transformations, and as a precursor for pyridine derivatives. Our product is rigorously tested to ensure ≥98% purity (HPLC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for medicinal chemistry, it serves as a key intermediate in the synthesis of bioactive molecules, ligands, and functional materials. Store in a cool, dry place at 2-8°C for prolonged shelf life.
Properties
- CAS Number: 30683-23-9
- Complexity: 140
- IUPAC Name: 3-bromopyridine-2-carboxylic acid
- InChI: InChI=1S/C6H4BrNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3H,(H,9,10)
- InChI Key: KBDIRPOTVAODSA-UHFFFAOYSA-N
- Exact Mass: 200.94254
- Molecular Formula: C6H4BrNO2
- Molecular Weight: 202.01
- SMILES: C1=CC(=C(N=C1)C(=O)O)Br
- Topological: 50.2
- Monoisotopic Mass: 200.94254
- Synonyms: 3-Bromopyridine-2-carboxylic Acid, 30683-23-9, DTXSID10365990, DTXCID10317030, 639-403-7, 3-bromopicolinic acid, 3-bromo-2-pyridinecarboxylic acid, 2-Pyridinecarboxylic acid, 3-bromo-, 3-Bromo-pyridine-2-carboxylic acid, MFCD01320380, 3-BROMOPYRIDINE-2-CARBOXYLICACID, F1926-0036, bromopyridine carboxylic, AF-399/40963066, SCHEMBL398923, bromopyridine-2-carboxylic acid, KBDIRPOTVAODSA-UHFFFAOYSA-N, 3-Bromopyridin-2-ylcarboxylic acid, SMSSF-0044124, 3-Bromo-2-pyridine carboxylic acid, BCP22115, BBL100607, SBB053041, STL554401, AKOS005198944, AC-3285, CS-W002771, FB19329, FS-1310, SB40495, 2-?Pyridinecarboxylic acid, 3-?bromo-, SY004667, EN300-84427, 3-Bromo-2-pyridinecarboxylic acid;3-Bromopicolinic acid, 3-Bromopicolinic acid pound>>2-Pyridinecarboxylic acid, 3-bromo-
Application
3-Bromopyridine-2-carboxylic Acid is widely used as a synthetic intermediate in the development of pharmaceuticals, particularly for kinase inhibitors and antiviral agents. It serves as a crucial precursor in Suzuki-Miyaura and Buchwald-Hartwig cross-coupling reactions to construct complex pyridine scaffolds. Researchers also employ it in coordination chemistry to design novel ligands for catalytic systems. Its carboxylic acid functionality allows for further derivatization via esterification or amidation, enabling diverse molecular architectures.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2A (100%)
- STOT SE 3 (100%)
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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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