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Catalog Number:
40181
CAS Number:
99349-68-5
Acide 3-acrylamidophénylboronique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Acide 3-acrylamidobenzèneboronique
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Product Information

3-Acrylamidophenylboronic acid is a versatile compound that combines the unique properties of boronic acids with the reactivity of acrylamides, making it an essential tool for researchers and industry professionals. This compound is particularly valuable in the development of sensors and drug delivery systems due to its ability to form reversible covalent bonds with diols, which enhances selectivity and sensitivity in various applications. Its structural features allow for the incorporation into polymer matrices, facilitating the design of smart materials that respond to environmental stimuli.

In the pharmaceutical industry, 3-Acrylamidophenylboronic acid is utilized in the synthesis of biologically active compounds and can serve as a key building block in the creation of targeted therapies. Its unique reactivity also makes it suitable for use in organic synthesis, particularly in the formation of complex molecular architectures. Researchers appreciate its potential in developing innovative solutions for diagnostics and therapeutics, highlighting its importance in advancing scientific knowledge and practical applications.

Synonyms
Acide 3-acrylamidobenzèneboronique
CAS Number
99349-68-5
Purity
≥ 97 % (HPLC)
Molecular Formula
C9H10BNO3
Molecular Weight
190.99
MDL Number
MFCD09025755
PubChem ID
10321331
Melting Point
146 °C (lit.)
Appearance
Poudre cristalline blanche à ambrée
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 3-acrylamidobenzèneboronique
CAS Number
99349-68-5
Purity
≥ 97 % (HPLC)
Molecular Formula
C9H10BNO3
Molecular Weight
190.99
MDL Number
MFCD09025755
PubChem ID
10321331
Melting Point
146 °C (lit.)
Appearance
Poudre cristalline blanche à ambrée
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

3-Acrylamidophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound is used in the synthesis of boronic acid derivatives that can enhance the efficacy of certain pharmaceuticals, particularly in cancer treatment.
  • Bioconjugation: It serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, which is crucial in developing targeted therapies.
  • Sensor Technology: The chemical is applied in the creation of sensors for detecting glucose and other biomolecules, making it valuable in diabetes management and medical diagnostics.
  • Polymer Chemistry: It is used in the production of smart polymers that respond to environmental stimuli, which can be applied in drug delivery systems and responsive materials.
  • Environmental Monitoring: This compound can be utilized in the detection of pollutants, aiding in environmental science and regulatory compliance by providing sensitive methods for monitoring water quality.

Citations