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5,7-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)quinoline

CAS 1815615-48-5Formula C15H16BF2NO2MW 291.1PubChem 123607240

5,7-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)quinoline is a fluorinated quinoline derivative featuring a pinacol boronate ester group. This compound serves as a versatile building block in organic synthesis, particularly for cross-coupling reactions, enabling the construction of complex molecular structures for research purposes.

Loading RDKit molecule structure...
InChIKey: SVTLXGSWLGDTDO-UHFFFAOYSA-NC15H16BF2NO2 | MW 291.1

Chemical Identity

Molecular Formula

C15H16BF2NO2

Molecular Weight

291.1 g/mol

Exact Mass

291.124215

PubChem CID

123607240

SMILES String

CC1(C)OB(c2ccnc3cc(F)cc(F)c23)OC1(C)C

External Identifiers
SCHEMBL17144750

Catalog Overview

This compound, 5,7-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)quinoline, is a meticulously designed functionalized intermediate for advanced chemical research. It incorporates a quinoline core substituted with two fluorine atoms at the 5 and 7 positions, enhancing its electronic properties. The presence of a 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) group makes it an excellent precursor for various palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura coupling. Researchers can utilize this compound to introduce a difluorinated quinoline moiety into target molecules, which is valuable in medicinal...

Use Context

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

This compound, 5,7-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)quinoline, is a meticulously designed functionalized intermediate for advanced chemical research. It incorporates a quinoline core substituted with two fluorine atoms at the 5 and 7 positions, enhancing its electronic properties. The presence of a 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) group makes it an excellent precursor for various palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura coupling. Researchers can utilize this compound to introduce a difluorinated quinoline moiety into target molecules, which is valuable in medicinal chemistry, agrochemical development, and materials science research. It is intended strictly for research and development use.

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

350.0 °C

Density

1.3 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 5,7-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)quinoline in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including safety goggles, gloves, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. Always consult the Safety Data Sheet (SDS) for comprehensive safety information and proper handling procedures before use. Store in a cool, dry place away from incompatible materials.

Related Products / Graph Discovery

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

Similar products (text references)

2710289-79-3CAS 2710289-79-3

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 293349GHS 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.