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Catalog Number:
40126
CAS Number:
373384-14-6
3-(Dimethylcarbamoyl)phenylboronic acid
Purity:
97 - 105 % (Assay by titration)
Synonym(s):
3-(Dimethylcarbamoyl)benzeneboronic acid
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Product Information

3-(Dimethylcarbamoyl)phenylboronic acid is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, enabling chemists to create complex molecules with precision. Researchers have utilized this compound in the synthesis of biologically active molecules, including potential anti-cancer agents and other therapeutic compounds, showcasing its relevance in drug discovery and development.

In addition to its synthetic utility, 3-(Dimethylcarbamoyl)phenylboronic acid serves as a crucial building block in the preparation of advanced materials and sensors. Its ability to participate in Suzuki-Miyaura cross-coupling reactions enhances its appeal in the field of materials science, where it contributes to the development of novel polymers and nanomaterials. This compound stands out for its efficiency and effectiveness in various applications, making it a valuable addition to any research or industrial laboratory focused on innovative chemical solutions.

Synonyms
3-(Dimethylcarbamoyl)benzeneboronic acid
CAS Number
373384-14-6
Purity
97 - 105 % (Assay by titration)
Molecular Formula
C9H12BNO3
Molecular Weight
193.01
MDL Number
MFCD03412066
PubChem ID
2773392
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-(Dimethylcarbamoyl)benzeneboronic acid
CAS Number
373384-14-6
Purity
97 - 105 % (Assay by titration)
Molecular Formula
C9H12BNO3
Molecular Weight
193.01
MDL Number
MFCD03412066
PubChem ID
2773392
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(Dimethylcarbamoyl)phenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted therapies for cancer treatment.
  • Organic Synthesis: It is employed in cross-coupling reactions, which are essential for constructing complex organic molecules, making it valuable in both academic and industrial laboratories.
  • Bioconjugation: The compound is used to create bioconjugates, enhancing the delivery of drugs or imaging agents to specific cells, thus improving therapeutic efficacy.
  • Material Science: It plays a role in the development of advanced materials, such as sensors and catalysts, due to its unique boronic acid functionality that can interact with various substrates.
  • Analytical Chemistry: This chemical is utilized in the development of analytical methods for detecting biomolecules, providing researchers with tools for better understanding biological processes.

Citations