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Catalog Number:
40108
CAS Number:
91983-14-1
Acide 2-(bromométhyl)phénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-(bromométhyl)benzèneboronique
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Product Information

2-(Bromomethyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable in the development of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique bromomethyl group enhances its reactivity, allowing for efficient functionalization and modification of aromatic compounds. Researchers and industry professionals can leverage this compound to create diverse chemical libraries and optimize drug candidates, particularly in the fields of cancer research and material science.

In addition to its synthetic applications, 2-(Bromomethyl)phenylboronic acid serves as an essential building block in the preparation of biologically active compounds. Its ability to form stable complexes with various substrates opens avenues for innovative research in drug discovery and development. The compound's stability and ease of handling further contribute to its appeal, making it a preferred choice for laboratories focused on high-throughput screening and compound optimization.

Synonyms
Acide 2-(bromométhyl)benzèneboronique
CAS Number
91983-14-1
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C7H8BBrO2
Molecular Weight
214.85
MDL Number
MFCD01318941
PubChem ID
2773278
Melting Point
138 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 2-(bromométhyl)benzèneboronique
CAS Number
91983-14-1
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C7H8BBrO2
Molecular Weight
214.85
MDL Number
MFCD01318941
PubChem ID
2773278
Melting Point
138 °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

2-(Bromomethyl)phenylboronic acid is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of anti-cancer drugs.
  • Cross-Coupling Reactions: It is extensively used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis, making it valuable in the production of complex organic molecules.
  • Material Science: The compound can be employed in the development of functional materials, such as polymers with specific electronic or optical properties, enhancing their performance in applications like sensors and displays.
  • Bioconjugation: It is useful in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in drug delivery systems and diagnostic applications.
  • Environmental Chemistry: This chemical can be applied in the development of sensors for detecting environmental pollutants, contributing to efforts in monitoring and improving air and water quality.

Citations