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Catalog Number:
40089
CAS Number:
91983-26-5
Acide 4-(cyanométhyl)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-(cyanométhyl)benzèneboronique
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Product Information

4-(Cyanomethyl)phenylboronic acid is a versatile compound widely utilized 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 Suzuki-Miyaura cross-coupling reactions. Researchers frequently employ this compound in the development of pharmaceuticals and agrochemicals, where its unique reactivity allows for the construction of complex molecular architectures. Its applications extend to the synthesis of biologically active compounds, including potential anticancer agents and other therapeutic molecules.

Additionally, 4-(Cyanomethyl)phenylboronic acid serves as a valuable building block in the preparation of functionalized materials and sensors. Its ability to participate in various coupling reactions enhances its utility in creating innovative materials for electronics and nanotechnology. With its favorable properties and broad applicability, this compound stands out as a key player in advancing research and development across multiple fields.

Synonyms
Acide 4-(cyanométhyl)benzèneboronique
CAS Number
91983-26-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C8H8BNO2
Molecular Weight
160.97
MDL Number
MFCD01632200
PubChem ID
2773342
Melting Point
191 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-(cyanométhyl)benzèneboronique
CAS Number
91983-26-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C8H8BNO2
Molecular Weight
160.97
MDL Number
MFCD01632200
PubChem ID
2773342
Melting Point
191 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-(Cyanomethyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the creation of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic structures, making it invaluable in drug development.
  • Bioconjugation: The boronic acid functionality allows for selective binding with diols, facilitating the development of bioconjugates for targeted drug delivery systems in cancer therapy.
  • Sensor Development: This compound can be utilized in the fabrication of chemical sensors that detect glucose levels, which is crucial for diabetes management and monitoring.
  • Material Science: It plays a role in the development of advanced materials, such as polymers and nanocomposites, enhancing properties like conductivity and mechanical strength.

Citations