Active Chemical RecordCatalog PreviewCatalog ready

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-bis(trifluoromethyl)pyridine

CAS 1320747-32-7Formula C13H14BF6NO2MW 341.06PubChem 89402037

This compound is a functionalized pyridine derivative containing a pinacol boronate ester and two trifluoromethyl groups. It is primarily used as a versatile building block in organic synthesis, particularly for C-C bond formation reactions, and for introducing specific electronic and steric properties into target molecules. Intended for Research Use Only (RUO).

Loading RDKit molecule structure...
InChIKey: BUORERSKCOUNGU-UHFFFAOYSA-NC13H14BF6NO2 | MW 341.06

Chemical Identity

Molecular Formula

C13H14BF6NO2

Molecular Weight

341.06 g/mol

Exact Mass

341.102178

PubChem CID

89402037

SMILES String

CC1(C)OB(c2cc(C(F)(F)F)nc(C(F)(F)F)c2)OC1(C)C

Names & Synonyms

C13H14BF6NO2BUORERSKCOUNGU-UHFFFAOYSA-NF5396002,6-Bis(trifluoromethyl)pyridine-4-boronic acid pinacol ester
External Identifiers
MFCD26516889SCHEMBL14678296AKOS037643818AS-37348

Catalog Overview

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-bis(trifluoromethyl)pyridine, with CAS 1320747-32-7, is a highly functionalized pyridine derivative. It features a pinacol boronate ester at the 4-position and two electron-withdrawing trifluoromethyl groups at the 2 and 6 positions of the pyridine ring. This unique combination of functionalities makes it a valuable intermediate in various synthetic routes. The boronate ester moiety is particularly useful for Suzuki-Miyaura cross-coupling reactions, enabling the formation of new carbon-carbon bonds with aryl or vinyl halides.

Use Context

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

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-bis(trifluoromethyl)pyridine, with CAS 1320747-32-7, is a highly functionalized pyridine derivative. It features a pinacol boronate ester at the 4-position and two electron-withdrawing trifluoromethyl groups at the 2 and 6 positions of the pyridine ring. This unique combination of functionalities makes it a valuable intermediate in various synthetic routes. The boronate ester moiety is particularly useful for Suzuki-Miyaura cross-coupling reactions, enabling the formation of new carbon-carbon bonds with aryl or vinyl halides. The trifluoromethyl groups can impart specific electronic and steric properties to target molecules, often enhancing metabolic stability or lipophilicity in drug discovery and agrochemical research. This compound is intended for Research Use Only (RUO).

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White to off-white crystalline powder

Physical State

Solid

Melting Point

110.0 °C

Boiling Point

305.0 °C

Density

1.5 g/cm³

Water Solubility

Insoluble

Flash Point

165.0 °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. Consult the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures.

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.