Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40194
CAS Number:
874219-36-0
3-(Ethoxycarbonyl)-4-fluorophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3-(Ethoxycarbonyl)-4-fluorobenzeneboronic acid
Documents
$106.96 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-(Ethoxycarbonyl)-4-fluorophenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds. Its unique structure, featuring a fluorine atom and an ethoxycarbonyl group, enhances its reactivity and selectivity, making it a preferred choice for researchers aiming to develop complex organic molecules, including pharmaceuticals and agrochemicals.

In addition to its synthetic applications, 3-(Ethoxycarbonyl)-4-fluorophenylboronic acid is also utilized in the development of targeted therapies, particularly in the field of cancer research, where boronic acids are known to interact with biological targets. Its favorable properties, such as high stability and solubility in various solvents, further support its use in diverse chemical environments. This compound stands out for its efficiency in facilitating reactions that lead to the synthesis of valuable intermediates, making it an indispensable tool for chemists and researchers alike.

Synonyms
3-(Ethoxycarbonyl)-4-fluorobenzeneboronic acid
CAS Number
874219-36-0
Purity
98 - 105% (Assay by titration)
Molecular Formula
C9H10BFO4
Molecular Weight
211.98
MDL Number
MFCD08061836
PubChem ID
24901771
Melting Point
152 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-(Ethoxycarbonyl)-4-fluorobenzeneboronic acid
CAS Number
874219-36-0
Purity
98 - 105% (Assay by titration)
Molecular Formula
C9H10BFO4
Molecular Weight
211.98
MDL Number
MFCD08061836
PubChem ID
24901771
Melting Point
152 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(Ethoxycarbonyl)-4-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 drugs targeting cancer and other diseases. Its boronic acid functionality allows for selective reactions that are crucial in medicinal chemistry.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds. This application is particularly valuable in the production of complex organic molecules, making it a staple in organic chemistry labs.
  • Material Science: The compound is used in the creation of advanced materials, including polymers and nanomaterials. Its unique properties enhance the performance of materials in electronics and coatings, offering improved durability and functionality.
  • Agricultural Chemistry: It finds applications in the synthesis of agrochemicals, such as herbicides and pesticides. The ability to modify its structure allows for the development of more effective and environmentally friendly agricultural products.
  • Diagnostic Tools: This chemical is also utilized in the development of diagnostic agents, particularly in imaging techniques. Its properties can be leveraged to improve the sensitivity and specificity of various diagnostic tests.

Citations