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Catalog Number:
26695
CAS Number:
1287753-36-9
Ácido {3-[1-(dimetilamino)etil]fenil}borónico
Purity:
≥ 95% (RMN)
Documents
$154.93 /100 mg
Tamaño
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Product Information

{3-[1-(Dimethylamino)ethyl]phenyl}boronic acid is a versatile compound widely utilized 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, which can enhance the efficiency of synthetic pathways in drug discovery and development. Researchers have successfully employed this compound in the synthesis of biologically active molecules, including potential anti-cancer agents and other therapeutic compounds, showcasing its relevance in the pharmaceutical industry.

In addition to its applications in drug synthesis, {3-[1-(Dimethylamino)ethyl]phenyl}boronic acid is also instrumental in the field of materials science, where it is used in the preparation of advanced materials and sensors. Its ability to participate in cross-coupling reactions further expands its utility in creating complex organic frameworks. With its favorable properties and broad applicability, this compound stands out as a valuable tool for researchers and industry professionals seeking innovative solutions in chemical synthesis and material development.

CAS Number
1287753-36-9
Purity
≥ 95% (RMN)
Molecular Formula
C10H16BNO2
Molecular Weight
193.1
MDL Number
MFCD08059973
PubChem ID
45791099
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1287753-36-9
Purity
≥ 95% (RMN)
Molecular Formula
C10H16BNO2
Molecular Weight
193.1
MDL Number
MFCD08059973
PubChem ID
45791099
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 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-[1-(Dimethylamino)ethyl]phenyl}boronic acid is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, enhancing the efficacy of drug formulations.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Organic Synthesis: The compound is used in organic synthesis reactions, particularly in cross-coupling reactions, which are essential for constructing complex organic molecules efficiently.
  • Sensor Technology: It finds applications in the development of chemical sensors, where its ability to interact with specific analytes can lead to the creation of sensitive detection systems for environmental monitoring.
  • Material Science: This boronic acid derivative is used in the formulation of advanced materials, including polymers that exhibit unique properties, such as improved thermal stability and mechanical strength.

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