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Catalog Number:
40191
CAS Number:
850589-53-6
Acide 3-éthoxy-5-fluorophénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-éthoxy-5-fluorobenzèneboronique
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$98.65 /200 mg
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Product Information

3-Ethoxy-5-fluorophenylboronic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued 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 structure, featuring both an ethoxy group and a fluorine atom, enhances its reactivity and selectivity, allowing researchers to develop targeted compounds with improved efficacy.

In addition to its synthetic applications, 3-Ethoxy-5-fluorophenylboronic acid has shown promise in the development of novel therapeutic agents, particularly in oncology, where it can be used to create compounds that inhibit cancer cell proliferation. Its compatibility with various reaction conditions and ease of handling make it an attractive choice for both academic and industrial laboratories. Researchers and professionals in the chemical industry will find this compound to be a valuable addition to their toolkit, facilitating the advancement of innovative solutions in drug discovery and development.

Synonyms
Acide 3-éthoxy-5-fluorobenzèneboronique
CAS Number
850589-53-6
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 10 BFO 3
Molecular Weight
183.97
MDL Number
MFCD07363779
PubChem ID
44558175
Melting Point
158 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-éthoxy-5-fluorobenzèneboronique
CAS Number
850589-53-6
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 10 BFO 3
Molecular Weight
183.97
MDL Number
MFCD07363779
PubChem ID
44558175
Melting Point
158 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-Ethoxy-5-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, due to its ability to form stable complexes with biomolecules.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential in creating complex organic molecules used in agrochemicals and materials science.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for drug delivery systems and targeted therapies.
  • Fluorescent Probes: Its unique fluorine substitution enhances the photophysical properties, making it suitable for developing fluorescent probes in biological imaging applications.
  • Research in Material Science: This compound is also explored in the development of new materials, such as polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.

Citations