C5H5BClNO2
157.36 g/mol
Research ReagentWarning
(2-chloropyridin-3-yl)boronic Acid
CAS381248-04-0
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound
(2-chloropyridin-3-yl)boronic acid is a boronic acid derivative commonly used as a research reagent in organic synthesis. Its structure features a pyridine ring with a chlorine substituent and a boronic acid group, making it a useful building block for cross-coupling reactions, particularly in medicinal chemistry research.
reagent for Suzuki-Miyaura coupling reactionsbuilding block in organic synthesisresearch compound for pharmaceutical intermediate studies
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
ReferenceSame Category
5-Bromo-3-chloro-2-fluoropyridine
CAS38185-56-7
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ReferenceSame Category
2-Chloro-5-fluoronicotinic acid
CAS38186-88-8
research compound
ReferenceSame Category
2-Bromo-5-fluoro-3-pyridinecarboxylic acid
CAS38186-89-9
research compound
ReferenceSame Category
Ethyl O-mesitylsulfonylacetohydroxamate
CAS38202-27-6
research compound
Safety Reference
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
(2-chloro-3-pyridinyl)boronic acid
InChIKey
VRDAOVQZVXYRNH-UHFFFAOYSA-N
SMILES
B(C1=C(N=CC=C1)Cl)(O)O
Synonyms (12)
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