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Catalog Number:
40169
CAS Number:
201802-29-1
[4-[Bis(4-methoxyphenyl)amino]phenyl]boronic acid
Purity:
98 - 105% (Assay by titration)
Documents
$377.97 /1G
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Product Information

[4-[Bis(4-methoxyphenyl)amino]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 form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for effective use in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Researchers have leveraged this compound in the synthesis of advanced materials and biologically active compounds, showcasing its relevance in both academic and industrial settings.

Moreover, [4-[Bis(4-methoxyphenyl)amino]phenyl]boronic acid stands out due to its enhanced solubility and stability compared to similar boronic acids, facilitating easier handling and application in laboratory environments. Its potential in drug discovery, particularly in the development of targeted therapies, highlights its importance in modern medicinal chemistry. With its robust performance in various synthetic pathways, this compound is an invaluable asset for researchers seeking to innovate in the fields of pharmaceuticals and materials science.

CAS Number
201802-29-1
Purity
98 - 105% (Assay by titration)
Molecular Formula
C20H20BNO4
Molecular Weight
349.19
MDL Number
MFCD28385171
PubChem ID
10569782
Appearance
White to light yellow crystalline powder
Conditions
Store at 2 - 8 °C
General Information
CAS Number
201802-29-1
Purity
98 - 105% (Assay by titration)
Molecular Formula
C20H20BNO4
Molecular Weight
349.19
MDL Number
MFCD28385171
PubChem ID
10569782
Appearance
White to light yellow crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

[4-[Bis(4-methoxyphenyl)amino]phenyl]boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in developing targeted cancer therapies. Its boronic acid functionality allows for specific interactions with biomolecules, enhancing drug efficacy.
  • Organic Electronics: It is used in the fabrication of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound's ability to facilitate charge transport makes it valuable in improving the performance of electronic devices.
  • Bioconjugation Chemistry: The unique properties of this compound enable its use in bioconjugation applications, where it can be linked to biomolecules for targeted delivery systems in drug development and diagnostics.
  • Sensor Technology: It is employed in developing chemical sensors due to its ability to selectively bind to certain analytes. This application is particularly useful in environmental monitoring and food safety testing.
  • Material Science: The compound is utilized in creating advanced materials with specific mechanical and thermal properties, making it suitable for applications in coatings and composites.

Citations