MolGraphChemical Intelligence
Active Chemical RecordCatalog PreviewCatalog ready

4-(1-Cyano-1-methylethyl)-2-fluorophenylboronic acid

CAS 1793003-65-2Formula C10H11BFNO2MW 207.01PubChem 74788322

4-(1-Cyano-1-methylethyl)-2-fluorophenylboronic acid is a fluorinated boronic acid derivative, commonly employed as a versatile building block in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions in research settings.

Loading RDKit molecule structure...
InChIKey: PYLDACORZHNYTJ-UHFFFAOYSA-NC10H11BFNO2 | MW 207.01

Chemical Identity

Molecular Formula

C10H11BFNO2

Molecular Weight

207.01 g/mol

Exact Mass

207.086687

PubChem CID

74788322

IUPAC Name

[4-(2-cyanopropan-2-yl)-2-fluorophenyl]boronic acid

SMILES String

CC(C)(C#N)c1ccc(B(O)O)c(F)c1

Names & Synonyms

[4-(1-cyano-1-methylethyl)-2-fluorophenyl]boronic acid(4-(2-cyanopropan-2-yl)-2-fluorophenyl)boronic acidF88212F6232664-(1-Cyano-1-methylethyl)-2-fluorophenylboronicacid
Show all synonyms
[4-(1-cyano-1-methyl-ethyl)-2-fluoro-phenyl]boronic acid
External Identifiers
MFCD22375016SCHEMBL30316138BS-31325CS-0178360

Catalog Overview

4-(1-Cyano-1-methylethyl)-2-fluorophenylboronic acid, identified by CAS 1793003-65-2, is an organic compound with the molecular formula C10H11BFNO2 and a molecular weight of 207. 01. This compound features a boronic acid group, a fluorine atom, and a cyanopropyl substituent attached to a phenyl ring. Its structural characteristics make it a valuable intermediate in the synthesis of complex organic molecules.

Use Context

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

4-(1-Cyano-1-methylethyl)-2-fluorophenylboronic acid, identified by CAS 1793003-65-2, is an organic compound with the molecular formula C10H11BFNO2 and a molecular weight of 207.01. This compound features a boronic acid group, a fluorine atom, and a cyanopropyl substituent attached to a phenyl ring. Its structural characteristics make it a valuable intermediate in the synthesis of complex organic molecules. Boronic acids are widely recognized for their utility in carbon-carbon bond formation, especially through palladium-catalyzed cross-coupling reactions like the Suzuki-Miyaura reaction, enabling the construction of diverse chemical scaffolds for research and development.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White to off-white crystalline powder

Physical State

Solid

Melting Point

150.0 °C

Boiling Point

300.0 °C

Density

1.3 g/cm³

Water Solubility

Slightly soluble

Flash Point

180.0 °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
  • For research use only. Handle 4-(1-Cyano-1-methylethyl)-2-fluorophenylboronic acid in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including gloves, eye protection, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. In case of contact, rinse immediately with plenty of water. Consult the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures. Store in a cool, dry place, away from incompatible materials.

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.