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2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)benzonitrile

CAS 1218791-15-1Formula C13H15BFNO2MW 247.07PubChem 53217116

A fluorinated benzonitrile derivative featuring a pinacol boronate ester, primarily used as a versatile building block in organic synthesis for research applications.

Loading RDKit molecule structure...
InChIKey: BDIHSSFYJYXWRV-UHFFFAOYSA-NC13H15BFNO2 | MW 247.07

Chemical Identity

Molecular Formula

C13H15BFNO2

Molecular Weight

247.07 g/mol

Exact Mass

247.117987

PubChem CID

53217116

SMILES String

CC1(C)OB(c2cccc(C#N)c2F)OC1(C)C

Names & Synonyms

3-Cyano-2-fluorophenylboronic acid pinacol ester3-Cyano-2-fluorophenylboronic acid, pinacol esterF694062Z20497620852-FLUORO-3-(TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZONITRILE
External Identifiers
MFCD11506358SCHEMBL19755529SCHEMBL29616950DTXSID60682220AKOS022183991AT16489MB09910BS-26600DB-366378CS-0174438EN300-7355322

Catalog Overview

2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)benzonitrile is a chemical compound characterized by a fluorinated benzonitrile core substituted with a 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl (pinacol boronate) group. This structure makes it a valuable functionalized intermediate in synthetic organic chemistry. The boronate ester moiety is particularly useful for carbon-carbon bond formation reactions, such as Suzuki-Miyaura cross-coupling, while the fluoro and cyano groups offer additional sites for further chemical transformations and introduce specific electronic properties. It is intended for research and...

Use Context

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

2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)benzonitrile is a chemical compound characterized by a fluorinated benzonitrile core substituted with a 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl (pinacol boronate) group. This structure makes it a valuable functionalized intermediate in synthetic organic chemistry. The boronate ester moiety is particularly useful for carbon-carbon bond formation reactions, such as Suzuki-Miyaura cross-coupling, while the fluoro and cyano groups offer additional sites for further chemical transformations and introduce specific electronic properties. It is intended for research and development purposes only.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White to off-white solid

Physical State

Solid

Melting Point

47.0 °C

Boiling Point

272.0 °C

Density

1.35 g/cm³

Water Solubility

1.32 × 10⁻³ mol/L

Flash Point

135.0 °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 under a 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 safety information before use. 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.

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 293190GHS Pictograms: GHS07Shipment review: Shipment details require review before fulfillment.

Compliance cues are non-linked reference tags and require shipment review.

Catalog navigation

Other public CAS pages in this catalog. These links support navigation across additional intermediates and do not imply equivalence, availability, or shared use.