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Catalog Number:
40117
CAS Number:
85107-53-5
Acide 2-(diméthylaminométhyl)phénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-(diméthylaminométhyl)benzèneboronique
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Product Information

2-(Dimethylaminomethyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique properties enable it to act as a key building block in the synthesis of biologically active compounds, including inhibitors for proteases and other enzymes. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, which are fundamental in creating complex organic molecules with precision and efficiency.

The compound's dimethylamino group enhances its reactivity and solubility, making it particularly valuable in diverse applications ranging from drug discovery to materials science. Its compatibility with various reaction conditions allows for flexibility in synthetic pathways, thereby streamlining the development of new therapeutic agents. With its proven efficacy in facilitating complex chemical transformations, 2-(Dimethylaminomethyl)phenylboronic acid stands out as a crucial tool for researchers and industry professionals aiming to innovate and enhance their chemical processes.

Synonyms
Acide 2-(diméthylaminométhyl)benzèneboronique
CAS Number
85107-53-5
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C9H14BNO2
Molecular Weight
179.03
MDL Number
MFCD01318999
PubChem ID
2734345
Melting Point
92 - 96 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide 2-(diméthylaminométhyl)benzèneboronique
CAS Number
85107-53-5
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C9H14BNO2
Molecular Weight
179.03
MDL Number
MFCD01318999
PubChem ID
2734345
Melting Point
92 - 96 °C
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

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

  • Drug Development: This compound serves as a crucial building block in the synthesis of pharmaceuticals, particularly in the development of targeted cancer therapies, enhancing the efficacy of drug candidates.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Organic Synthesis: The compound is used in various organic synthesis reactions, particularly in the formation of carbon-boron bonds, which are valuable in creating complex organic molecules.
  • Sensor Technology: Its unique properties make it suitable for developing sensors that detect specific biomolecules, aiding in diagnostics and environmental monitoring.
  • Material Science: This chemical is applied in the development of advanced materials, such as polymers and composites, which can enhance the performance of products in various industries.

Citations