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Catalog Number:
26697
CAS Number:
1256355-44-8
Ácido [3-(1-pirrolidin-1-iletil)fenil]borónico
Purity:
≥ 95% (RMN)
Documents
$93.14 /1G
Tamaño
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Product Information

[3-(1-Pyrrolidin-1-ylethyl)phenyl]boronic acid is a versatile compound with significant applications in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura coupling reactions, making it an essential building block for the formation of biaryl compounds. Its unique structure, featuring a pyrrolidine moiety, enhances its reactivity and selectivity, which is particularly valuable in the development of pharmaceuticals and agrochemicals. Researchers have utilized this compound in the synthesis of various biologically active molecules, demonstrating its potential in drug discovery and development.

In addition to its synthetic utility, [3-(1-Pyrrolidin-1-ylethyl)phenyl]boronic acid exhibits properties that may contribute to improved solubility and bioavailability of target compounds. This characteristic is crucial for enhancing the efficacy of therapeutic agents. Its application in the field of materials science, particularly in the development of functional polymers and sensors, further underscores its versatility. With its favorable properties and broad range of applications, this compound is an excellent choice for researchers and industry professionals seeking reliable and effective solutions in their projects.

CAS Number
1256355-44-8
Purity
≥ 95% (RMN)
Molecular Formula
C12H18BNO2
Molecular Weight
219.1
MDL Number
MFCD09864340
PubChem ID
45791103
Appearance
Sólido amarillo
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1256355-44-8
Purity
≥ 95% (RMN)
Molecular Formula
C12H18BNO2
Molecular Weight
219.1
MDL Number
MFCD09864340
PubChem ID
45791103
Appearance
Sólido amarillo
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-Pyrrolidin-1-ylethyl)phenyl]boronic acid is widely utilized in research focused on:

  • Medicinal Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and diabetes.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, facilitating the formation of carbon-carbon bonds, which is crucial in creating complex organic molecules.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing their properties for applications in electronics and coatings.
  • Biochemistry: It acts as a tool for studying protein interactions and enzyme activities, providing insights into biological processes and aiding in drug discovery.
  • Analytical Chemistry: This boronic acid derivative is utilized in sensor technology for detecting sugars and other biomolecules, offering high sensitivity and specificity in various analytical applications.

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