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Catalog Number:
40340
CAS Number:
156487-12-6
Ácido 4-butoxi-2,3-difluorofenilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-butoxi-2,3-difluorobencenoborónico
Documents
$138.71 /1G
Tamaño
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Product Information

4-Butoxy-2,3-difluorophenylboronic acid is a versatile boronic acid derivative known for its unique reactivity and utility in organic synthesis. This compound features a butoxy group and two fluorine atoms on the aromatic ring, enhancing its electrophilic properties, making it an excellent candidate for Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals can leverage this compound in the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to form stable complexes with various substrates allows for the synthesis of complex molecules with precision and efficiency.

In addition to its synthetic applications, 4-butoxy-2,3-difluorophenylboronic acid is valuable in the field of medicinal chemistry, where it can be utilized in the design of targeted therapies and drug discovery processes. Its favorable solubility and stability under various conditions make it an ideal choice for laboratory experiments and industrial applications alike. With its distinctive properties, this compound stands out as a reliable building block for innovative chemical research and development.

Synonyms
Ácido 4-butoxi-2,3-difluorobencenoborónico
CAS Number
156487-12-6
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C10H13BF2O3
Molecular Weight
230.02
MDL Number
MFCD19441186
PubChem ID
54132493
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-butoxi-2,3-difluorobencenoborónico
CAS Number
156487-12-6
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C10H13BF2O3
Molecular Weight
230.02
MDL Number
MFCD19441186
PubChem ID
54132493
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Butoxy-2,3-difluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is crucial in synthesizing various pharmaceuticals, particularly in creating boronate esters that are essential for drug formulation.
  • Organic Synthesis: It serves as a versatile building block in organic synthesis, allowing chemists to create complex molecules efficiently, which is particularly beneficial in the field of medicinal chemistry.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is vital in developing targeted drug delivery systems.
  • Material Science: It finds applications in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and strength.
  • Fluorescent Probes: This chemical is employed in creating fluorescent probes for biological imaging, helping researchers visualize cellular processes with high specificity and sensitivity.

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