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3-Fluoro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine

CAS 1984826-57-4Formula C12H14BF4NO2MW 291.05PubChem 123860100

This compound is a fluorinated pyridine derivative featuring a trifluoromethyl group and a pinacol boronate ester. It serves as a versatile building block in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions in research settings.

Loading RDKit molecule structure...
InChIKey: QVUUYXCNDUEIRV-UHFFFAOYSA-NC12H14BF4NO2 | MW 291.05

Chemical Identity

Molecular Formula

C12H14BF4NO2

Molecular Weight

291.05 g/mol

Exact Mass

291.105372

PubChem CID

123860100

IUPAC Name

3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine

SMILES String

CC1(C)OB(c2cnc(C(F)(F)F)c(F)c2)OC1(C)C

Names & Synonyms

817-345-5F780111Z21816524285-Fluoro-6-(trifluoromethyl)pyridine-3-boronic Acid Pinacol Ester(5-FLUORO-6-(TRIFLUOROMETHYL)PYRIDIN-3-YL)BORONIC ACID PINACOL ESTER
External Identifiers
RefChem:501829SCHEMBL16647939JED82657AT25125SY479467CS-0502075EN300-1272282

Catalog Overview

3-Fluoro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine is a highly functionalized pyridine intermediate. It incorporates a fluorine atom, a trifluoromethyl group, and a pinacol boronate ester moiety. The boronate ester group makes it an excellent reagent for carbon-carbon bond formation, such as in Suzuki-Miyaura coupling reactions, enabling the introduction of the fluorinated pyridine scaffold into more complex molecular structures. The trifluoromethyl group often imparts unique electronic and steric properties, which can be beneficial in medicinal chemistry and material science research.

Use Context

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

3-Fluoro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine is a highly functionalized pyridine intermediate. It incorporates a fluorine atom, a trifluoromethyl group, and a pinacol boronate ester moiety. The boronate ester group makes it an excellent reagent for carbon-carbon bond formation, such as in Suzuki-Miyaura coupling reactions, enabling the introduction of the fluorinated pyridine scaffold into more complex molecular structures. The trifluoromethyl group often imparts unique electronic and steric properties, which can be beneficial in medicinal chemistry and material science research. This compound is valuable for researchers synthesizing novel fluorinated compounds.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white solid

Physical State

solid

Melting Point

97.0 °C

Boiling Point

242.0 °C

Density

1.4 g/cm³

Water Solubility

6.03 × 10⁻⁴ mol/L

Flash Point

115.0 °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 (PPE) including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood. Avoid inhalation, ingestion, and skin contact. Refer to the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures. Store in a cool, dry place, tightly sealed.

Related Products / Graph Discovery

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

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