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

Catalog Number:
40197
CAS Number:
122775-35-3
Ácido 3,4-dimetoxifenilborónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 3,4-dimetoxibencenoborónico
Documents
$18.50 /5G
Tamaño
Request Bulk Quote
Product Information

3,4-Dimethoxyphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its unique structure, featuring two methoxy groups, enhances its solubility and reactivity, allowing for efficient coupling with various electrophiles. Researchers and industry professionals utilize 3,4-Dimethoxyphenylboronic acid in the development of pharmaceuticals, agrochemicals, and advanced materials, where it serves as a key building block in the synthesis of complex organic molecules.

In addition to its synthetic applications, this compound is also explored for its potential in biological studies, particularly in the development of targeted therapies. Its ability to selectively bind to specific biomolecules opens avenues for innovative drug design and delivery systems. With its favorable properties and broad applicability, 3,4-Dimethoxyphenylboronic acid stands out as a valuable tool for chemists seeking to enhance their research and development efforts.

Synonyms
Ácido 3,4-dimetoxibencenoborónico
CAS Number
122775-35-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 8 H 11 BO 4
Molecular Weight
181.98
MDL Number
MFCD01074574
PubChem ID
2734702
Melting Point
245 - 250 °C
Appearance
Polvo blanquecino
Conditions
Tienda en RT
General Information
Synonyms
Ácido 3,4-dimetoxibencenoborónico
CAS Number
122775-35-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 8 H 11 BO 4
Molecular Weight
181.98
MDL Number
MFCD01074574
PubChem ID
2734702
Melting Point
245 - 250 °C
Appearance
Polvo blanquecino
Conditions
Tienda en RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3,4-Dimethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in creating complex organic molecules.
  • Pharmaceutical Development: It plays a significant role in drug discovery and development, particularly in the synthesis of biologically active compounds, enhancing the efficiency of creating new medications.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings due to their unique properties.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in the development of biosensors and targeted drug delivery systems.
  • Analytical Chemistry: This chemical is utilized in various analytical methods, including chromatography and spectroscopy, to improve the detection and quantification of compounds in complex mixtures.

Citas