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Catalog Number:
26261
CAS Number:
760990-08-7
Ester pinacol de l'acide 4-fluoro-3-hydroxyphénylboronique
Purity:
≥ 98% (CG)
Documents
$58.39 /250 mg
Taille
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Product Information

4-Fluoro-3-hydroxyphenylboronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique fluorine substituent enhances its reactivity and selectivity, allowing for the development of targeted therapies and advanced materials.

Researchers and industry professionals appreciate this compound for its stability and ease of handling, which facilitate various applications in drug discovery and development. The pinacol ester form provides improved solubility and compatibility with a range of solvents, making it ideal for high-throughput screening and other laboratory processes. With its favorable properties, 4-Fluoro-3-hydroxyphenylboronic acid pinacol ester stands out as a crucial reagent for innovative chemical research and development.

CAS Number
760990-08-7
Purity
≥ 98% (CG)
Molecular Formula
C 12 H 16 BFO 3
Molecular Weight
238.06
MDL Number
MFCD16994403
PubChem ID
11572238
Melting Point
83-92 ?C
Appearance
Solide blanc à brun clair
Conditions
Conserver à 0-8°C
General Information
CAS Number
760990-08-7
Purity
≥ 98% (CG)
Molecular Formula
C 12 H 16 BFO 3
Molecular Weight
238.06
MDL Number
MFCD16994403
PubChem ID
11572238
Melting Point
83-92 ?C
Appearance
Solide blanc à brun clair
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Fluoro-3-hydroxyphenylboronic acid pinacol ester is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing pharmaceuticals, particularly in developing targeted therapies for cancer and other diseases.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems.
  • Organic Synthesis: This chemical plays a crucial role in organic synthesis, particularly in creating complex organic molecules through cross-coupling reactions, which are essential in materials science.
  • Fluorescent Probes: It can be utilized to develop fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Sensor Technology: The compound is applicable in the development of sensors for detecting specific biomolecules, offering advantages in sensitivity and selectivity compared to traditional methods.

Citations