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Catalog Number:
40076
CAS Number:
4612-26-4
Ácido 1,4-fenilendiborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 1,4-bencenodiborónico
Documents
$36.65 /1G
Tamaño
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Product Information

1,4-Phenylenediboronic acid is a versatile compound widely utilized in organic synthesis and materials science. This compound, also known as 4,4'-Dihydroxy-1,1'-biphenyl-2,2'-diylboronic acid, features two boronic acid functional groups that enhance its reactivity and make it an invaluable building block for the development of complex organic molecules. Its unique structure allows for effective cross-coupling reactions, particularly in the synthesis of biaryl compounds, which are crucial in pharmaceuticals and agrochemicals.

In addition to its role in organic synthesis, 1,4-Phenylenediboronic acid is increasingly employed in the field of sensor technology and drug delivery systems due to its ability to form stable complexes with diols. This property is particularly beneficial in the design of biosensors and targeted drug delivery mechanisms, where specificity and stability are paramount. Researchers and industry professionals can leverage the compound's reactivity and functional versatility to innovate in various applications, from developing new materials to enhancing existing chemical processes.

Synonyms
Ácido 1,4-bencenodiborónico
CAS Number
4612-26-4
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C6H8B2O4
Molecular Weight
165.75
MDL Number
MFCD00236018
PubChem ID
230478
Melting Point
> 300 °C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 1,4-bencenodiborónico
CAS Number
4612-26-4
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C6H8B2O4
Molecular Weight
165.75
MDL Number
MFCD00236018
PubChem ID
230478
Melting Point
> 300 °C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,4-Phenylenediboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in creating complex organic structures.
  • Polymer Chemistry: The compound is used in the production of boron-containing polymers, which exhibit unique properties such as increased thermal stability and improved mechanical strength.
  • Sensor Development: Its ability to form complexes with various analytes makes it valuable in developing chemical sensors for detecting biomolecules and environmental pollutants.
  • Bioconjugation: 1,4-Phenylenediboronic acid is utilized in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in drug delivery and diagnostics.

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