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· · COA & SDS available for every product · Same-day shipping on in-stock items 5-Bromopyridine-3-carboxylic acid - ≥99% , CAS No.20826-04-4
Synonyms
5-Bromonicotinic acid | 5-bromo-nicotinic acid | 5-Bromopyridine-3-carboxylic acid | 5-Bromo-3-pyridinecarboxylic acid | 3-bromo-5-pyridine carboxylic acid
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Why this grade ≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Product Application：
5-Bromopyridine-3-carboxylic acid (5-bromonicotinic acid) was used in the synthesis of 3-guanidinomethyl-5-iodopyridine.
Specifications Synonyms
5-Bromonicotinic acid | 5-bromo-nicotinic acid | 5-Bromopyridine-3-carboxylic acid | 5-Bromo-3-pyridinecarboxylic acid | 3-bromo-5-pyridine carboxylic acid
Specifications & Purity
≥99%
Names and Identifiers Pubchem Sid 488186514 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488186514 Canonical Smiles C1=C(C=NC=C1Br)C(=O)O IUPAC Name 5-bromopyridine-3-carboxylic acid InChIKey FQIUCPGDKPXSLL-UHFFFAOYSA-N INCHI 1S/C6H4BrNO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3H,(H,9,10) Isomeric SMILES C1=C(C=NC=C1Br)C(=O)O WGK Germany 3 RTECS QT0868000 Molecular Weight 202.01 Beilstein 115854 Reaxy-Rn 115854 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=115854&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Pyridines and derivatives Subclass Pyridinecarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Pyridinecarboxylic acids Alternative Parents Aryl bromides Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Pyridine carboxylic acid - Aryl bromide - Aryl halide - Heteroaromatic compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as pyridinecarboxylic acids. These are compounds containing a pyridine ring bearing a carboxylic acid group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Melt Point(°C) 182-186°C Molecular Weight 202.010 g/mol XLogP3 1.100 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 200.943 Da Monoisotopic Mass 200.943 Da Topological Polar Surface Area 50.200 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 140.000 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
Citations of This Product References 1. Yafang Ge, Guoting Li, Dongxia Fu, Lina Liu, Benlai Wu. (2019) Manganese(II) and zinc(II) coordination polymers based on 2-(5-bromo-pyridin-3-yl)-1H-imidazole-4,5-dicarboxylic acid: synthesis, structure and properties. JOURNAL OF COORDINATION CHEMISTRY, [PMID: [10.1080/00958972.2019.1638509 ]
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