Active Chemical RecordCatalog PreviewCatalog ready

2-Fluoro-5-(trifluoromethyl)pyridin-3-ylboronic acid

CAS 1253569-51-5Formula C6H4BF4NO2MW 208.91PubChem 53484303

2-Fluoro-5-(trifluoromethyl)pyridin-3-ylboronic acid is a boronic acid derivative featuring a fluorinated pyridine ring with a trifluoromethyl group. It is primarily used as a versatile building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing complex molecules in research settings.

Loading RDKit molecule structure...
InChIKey: PVDFJVJLKFKDGJ-UHFFFAOYSA-NC6H4BF4NO2 | MW 208.91

Chemical Identity

Molecular Formula

C6H4BF4NO2

Molecular Weight

208.91 g/mol

Exact Mass

209.027121

PubChem CID

53484303

IUPAC Name

[2-fluoro-5-(trifluoromethyl)-3-pyridinyl]boronic acid

SMILES String

OB(O)c1cc(C(F)(F)F)cnc1F

Names & Synonyms

2-fluoro-5-(trifluoromethyl)pyridine-3-boronic acid(2-fluoro-5-(trifluoromethyl)pyridin-3-yl)boronic acid[2-fluoro-5-(trifluoromethyl)pyridin-3-yl]boronic acidPVDFJVJLKFKDGJ-UHFFFAOYSA-NF622949
Show all synonyms
2-Fluoro-5-(trifluoromethyl)pyridin-3-ylboronicacid[2-fluoro-5-(trifluoromethyl)-3-pyridyl]boronic acid
External Identifiers
MFCD16140228SCHEMBL3108377SCHEMBL29957490AKOS025293597AT15221BS-30402SY226982CS-0178028EN300-2345513

Catalog Overview

2-Fluoro-5-(trifluoromethyl)pyridin-3-ylboronic acid, identified by CAS 1253569-51-5, is a highly functionalized boronic acid. Its structure incorporates a pyridine core substituted with a fluorine atom at position 2 and a trifluoromethyl group at position 5, with the boronic acid moiety at position 3. This combination of functional groups makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The boronic acid group is highly reactive in palladium-catalyzed cross-coupling reactions, while the fluorine and trifluoromethyl groups can impart specific electronic and steric...

Use Context

  • Research chemical sourcing
  • Custom synthesis and catalog availability review
  • COA, SDS, pricing, and fulfillment workflow
Read more catalog context

2-Fluoro-5-(trifluoromethyl)pyridin-3-ylboronic acid, identified by CAS 1253569-51-5, is a highly functionalized boronic acid. Its structure incorporates a pyridine core substituted with a fluorine atom at position 2 and a trifluoromethyl group at position 5, with the boronic acid moiety at position 3. This combination of functional groups makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The boronic acid group is highly reactive in palladium-catalyzed cross-coupling reactions, while the fluorine and trifluoromethyl groups can impart specific electronic and steric properties to the final compounds, influencing their biological activity or material properties. It is typically supplied as a research-use-only chemical.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White to off-white crystalline powder

Physical State

Solid

Melting Point

120.0 °C

Boiling Point

300.0 °C

Density

1.6 g/cm³

Water Solubility

Slightly soluble

Flash Point

170.0 °C

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Refer to the Safety Data Sheet (SDS) for comprehensive safety information. This product is for research use only and not for human or animal therapeutic or diagnostic use.

Related Products / Graph Discovery

Related products, derivatives, keywords, and application cues for catalog discovery.

Related products and analog discovery will be available as catalog graph data is expanded.