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Catalog Number:
40150
CAS Number:
150255-96-2
3-Cyanophenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Cyanobenzeneboronic acid
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Product Information

3-Cyanophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a cyano group, enhancing its reactivity and making it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique properties allow for the formation of stable complexes with diols, which is particularly beneficial in the synthesis of various biologically active compounds. Researchers have effectively employed 3-Cyanophenylboronic acid in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of complex molecular architectures that are pivotal in drug discovery and development.

In addition to its applications in synthetic chemistry, 3-Cyanophenylboronic acid has shown promise in the field of sensor technology, where it can be used to detect specific biomolecules due to its ability to form reversible covalent bonds. This compound stands out for its ease of use and compatibility with various reaction conditions, making it a preferred choice for chemists seeking efficient and effective synthetic pathways. Its role in advancing research and development in pharmaceuticals and materials science underscores its significance in contemporary chemical applications.

Synonyms
3-Cyanobenzeneboronic acid
CAS Number
150255-96-2
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BNO2
Molecular Weight
146.94
MDL Number
MFCD01318967
PubChem ID
2734325
Melting Point
298 °C (dec.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Cyanobenzeneboronic acid
CAS Number
150255-96-2
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BNO2
Molecular Weight
146.94
MDL Number
MFCD01318967
PubChem ID
2734325
Melting Point
298 °C (dec.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Cyanophenylboronic 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.
  • Drug Development: Its ability to form reversible covalent bonds with biomolecules makes it valuable in designing targeted drug delivery systems, enhancing the efficacy of therapeutic agents.
  • Materials Science: Used in the production of advanced materials, particularly in the creation of polymers and nanomaterials that exhibit unique electrical and optical properties.
  • Bioconjugation: This compound is utilized in bioconjugation techniques, aiding in the labeling of proteins and nucleic acids for research in molecular biology and diagnostics.
  • Sensor Technology: Its properties allow for the development of sensors that can detect specific biological or chemical substances, making it useful in environmental monitoring and medical diagnostics.

Citations