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Catalog Number:
40291
CAS Number:
874219-60-0
5-(Ethoxycarbonyl)-2-fluorophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
5-(Ethoxycarbonyl)-2-fluorobenzeneboronic acid
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$87.53 /200MG
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Product Information

5-(Ethoxycarbonyl)-2-fluorophenylboronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds. Its unique structure, featuring both a boronic acid functional group and an ethoxycarbonyl moiety, enhances its reactivity and selectivity in various chemical transformations. Researchers and industry professionals can leverage this compound in the development of complex pharmaceuticals, agrochemicals, and advanced materials.

In addition to its synthetic applications, 5-(Ethoxycarbonyl)-2-fluorophenylboronic acid has shown promise in the field of drug discovery, particularly in the design of targeted therapies. Its fluorine atom contributes to increased metabolic stability and bioactivity, making it a candidate for further exploration in medicinal applications. With its unique properties and practical uses, this compound stands out as a valuable tool for chemists seeking to innovate in their respective fields.

Synonyms
5-(Ethoxycarbonyl)-2-fluorobenzeneboronic acid
CAS Number
874219-60-0
Purity
98 - 105% (Assay by titration)
Molecular Formula
C9H10BFO4
Molecular Weight
211.98
MDL Number
MFCD08235094
PubChem ID
44717604
Melting Point
99 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
5-(Ethoxycarbonyl)-2-fluorobenzeneboronic acid
CAS Number
874219-60-0
Purity
98 - 105% (Assay by titration)
Molecular Formula
C9H10BFO4
Molecular Weight
211.98
MDL Number
MFCD08235094
PubChem ID
44717604
Melting Point
99 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-(Ethoxycarbonyl)-2-fluorophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of targeted therapies for cancer treatment.
  • Chemical Synthesis: It is employed in cross-coupling reactions, which are essential for constructing complex organic molecules, making it valuable in both academic and industrial chemistry.
  • Material Science: The compound is used in the creation of advanced materials, such as polymers and nanomaterials, enhancing properties like strength and thermal stability.
  • Bioconjugation: It facilitates the attachment of biomolecules in bioconjugation processes, which is crucial for developing diagnostic tools and targeted drug delivery systems.
  • Research on Fluorinated Compounds: Its unique fluorine atom allows researchers to study the effects of fluorination on biological activity, aiding in the design of more effective compounds.

Citations