Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
28627
CAS Number:
214360-73-3
4-Aminophenyl)boronic acid pinacol ester
Purity:
≥ 99% (GC)
Documents
$18.53 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

(4-Aminophenyl)boronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a boronate ester that enhances its reactivity, making it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique structure allows for efficient coupling reactions, particularly in Suzuki-Miyaura cross-coupling, which is pivotal for constructing complex organic molecules. Researchers appreciate its ability to facilitate the formation of carbon-carbon bonds, thus streamlining the synthesis of various biologically active compounds.

In addition to its synthetic applications, (4-Aminophenyl)boronic acid pinacol ester has shown promise in the development of targeted therapies, particularly in oncology, where boron-containing compounds are being explored for their potential in boron neutron capture therapy (BNCT). Its favorable properties, such as stability and solubility, make it an attractive choice for researchers looking to innovate in drug design and development. This compound not only enhances the efficiency of synthetic pathways but also opens new avenues for therapeutic applications, making it a valuable asset in both academic and industrial settings.

CAS Number
214360-73-3
Purity
≥ 99% (GC)
Molecular Formula
C12H18BNO2
Molecular Weight
219.09
MDL Number
MFCD02093721
PubChem ID
2734620
Appearance
Yellow to brown solid
Conditions
Store at 0-8°C
General Information
CAS Number
214360-73-3
Purity
≥ 99% (GC)
Molecular Formula
C12H18BNO2
Molecular Weight
219.09
MDL Number
MFCD02093721
PubChem ID
2734620
Appearance
Yellow to brown solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(4-Aminophenyl)boronic acid pinacol ester is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing pharmaceuticals, particularly in developing targeted therapies for cancer, due to its ability to interact with biological molecules effectively.
  • Organic Synthesis: It is employed in various organic reactions, including Suzuki coupling, which allows for the formation of carbon-carbon bonds, essential in creating complex organic molecules.
  • Materials Science: The compound is used in the production of advanced materials, such as polymers and nanomaterials, enhancing properties like conductivity and strength, which are crucial in electronics and aerospace industries.
  • Bioconjugation: Its unique functional groups enable bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other compounds, which is vital in developing biosensors and diagnostic tools.
  • Research in Catalysis: This ester plays a role in catalysis research, helping scientists explore new catalytic processes that can lead to more efficient chemical reactions, thereby reducing waste and energy consumption.

Citations