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Catalog Number:
40258
CAS Number:
603122-84-5
Ácido 2-fluoro-4-(metoxicarbonil)fenilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 2-fluoro-4-(metoxicarbonil)bencenoborónico
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Product Information

2-Fluoro-4-(methoxycarbonyl)phenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the development of complex organic molecules. Its unique fluorine substituent enhances its reactivity and selectivity, allowing researchers to create diverse functionalized compounds with precision.

In pharmaceutical research, 2-Fluoro-4-(methoxycarbonyl)phenylboronic acid is particularly valuable for the synthesis of biologically active molecules, including potential drug candidates. Its application extends to the development of agrochemicals and materials science, where it can be utilized in the creation of novel polymers and advanced materials. With its favorable properties and broad applicability, this compound is an indispensable tool for researchers and industry professionals seeking to innovate and enhance their product offerings.

Synonyms
Ácido 2-fluoro-4-(metoxicarbonil)bencenoborónico
CAS Number
603122-84-5
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C8H8BFO4
Molecular Weight
197.96
MDL Number
MFCD08436034
PubChem ID
24824345
Melting Point
140 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 2-fluoro-4-(metoxicarbonil)bencenoborónico
CAS Number
603122-84-5
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C8H8BFO4
Molecular Weight
197.96
MDL Number
MFCD08436034
PubChem ID
24824345
Melting Point
140 °C (Literatura)
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

2-Fluoro-4-(methoxycarbonyl)phenylboronic 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. Its unique boronic acid functionality allows for selective reactions that enhance drug efficacy.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for forming carbon-carbon bonds. This application is crucial in the creation of complex organic molecules used in materials science and medicinal chemistry.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems and diagnostic tools in biomedicine.
  • Material Science: Its properties make it suitable for creating functionalized polymers and materials, which can be used in electronics and sensors, providing enhanced performance compared to traditional materials.
  • Research in Catalysis: The compound acts as a catalyst in various chemical reactions, improving reaction rates and selectivity, which is beneficial for researchers looking to optimize synthetic pathways.

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