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Catalog Number:
40112
CAS Number:
123088-59-5
Acide 4-carbamoylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-carbamoylbenzèneboronique
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Product Information

4-Carbamoylphenylboronic acid is a versatile compound recognized for its unique boronic acid functionality, making it an essential building block in organic synthesis and medicinal chemistry. This compound features a carbamoyl group that enhances its reactivity and solubility, allowing it to participate in various coupling reactions, such as Suzuki-Miyaura cross-coupling. Researchers and industry professionals can leverage its properties for the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to form stable complexes with diols also positions it as a valuable tool in sensor technology and biomolecular studies.

In addition to its synthetic applications, 4-Carbamoylphenylboronic acid is noteworthy for its potential use in drug discovery, particularly in the design of inhibitors targeting specific enzymes. Its compatibility with various reaction conditions and ease of functionalization make it a preferred choice for chemists seeking to innovate in their research. With its broad applicability and unique features, this compound stands out as a key reagent in the toolkit of modern chemistry.

Synonyms
Acide 4-carbamoylbenzèneboronique
CAS Number
123088-59-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C7H8BNO3
Molecular Weight
164.96
MDL Number
MFCD03411940
PubChem ID
2737811
Melting Point
234 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 4-carbamoylbenzèneboronique
CAS Number
123088-59-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C7H8BNO3
Molecular Weight
164.96
MDL Number
MFCD03411940
PubChem ID
2737811
Melting Point
234 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Carbamoylphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing pharmaceuticals, particularly in developing drugs targeting cancer and diabetes.
  • Bioconjugation: It is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Organic Synthesis: The compound plays a significant role in organic synthesis, particularly in cross-coupling reactions, which are essential for creating complex organic molecules.
  • Sensor Technology: It is applied in developing sensors for detecting biomolecules, offering high sensitivity and specificity, which is crucial for medical diagnostics.
  • Material Science: The compound is utilized in creating advanced materials, such as polymers and coatings, that require specific chemical properties for improved performance.

Citations