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Catalog Number:
40184
CAS Number:
405520-68-5
Acide 4-(diméthylcarbamoyl)phénylboronique
Purity:
94 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-(diméthylcarbamoyl)benzèneboronique
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Product Information

4-(Dimethylcarbamoyl)phenylboronic acid is a versatile compound known for its significant role in organic synthesis and medicinal chemistry. This boronic acid derivative features a dimethylcarbamoyl group, enhancing its reactivity and making it a valuable building block in the development of pharmaceuticals and agrochemicals. Its unique properties allow it to participate in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in complex organic molecules. This makes it particularly useful in the synthesis of biologically active compounds, including potential drug candidates and advanced materials.

Researchers and industry professionals can leverage 4-(Dimethylcarbamoyl)phenylboronic acid for its ability to facilitate the creation of intricate molecular architectures. Its application extends to the development of targeted therapies and novel agrochemical products, where precision and efficiency are paramount. The compound's stability and compatibility with various reaction conditions further enhance its appeal, making it a preferred choice for those seeking reliable and effective solutions in their synthetic endeavors.

Synonyms
Acide 4-(diméthylcarbamoyl)benzèneboronique
CAS Number
405520-68-5
Purity
94 - 105 % (dosage par titrage)
Molecular Formula
C9H12BNO3
Molecular Weight
193.01
MDL Number
MFCD02258943
PubChem ID
3503767
Melting Point
145 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 4-(diméthylcarbamoyl)benzèneboronique
CAS Number
405520-68-5
Purity
94 - 105 % (dosage par titrage)
Molecular Formula
C9H12BNO3
Molecular Weight
193.01
MDL Number
MFCD02258943
PubChem ID
3503767
Melting Point
145 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
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-(Dimethylcarbamoyl)phenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound plays a critical role in the synthesis of boron-containing pharmaceuticals, enhancing the efficacy of drug candidates in treating various diseases.
  • Chemical Synthesis: It serves as a versatile building block in organic synthesis, particularly in the formation of complex molecules, making it valuable for chemists in both academic and industrial settings.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in developing targeted therapies and diagnostics.
  • Material Science: In the field of material science, it contributes to the development of advanced materials with unique properties, such as improved conductivity or enhanced mechanical strength.
  • Analytical Chemistry: This chemical is utilized in analytical methods for detecting and quantifying specific compounds, providing researchers with reliable tools for quality control and environmental monitoring.

Citations