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Catalog Number:
31434
CAS Number:
99768-12-4
4-Methoxycarbonylphenylboronic acid
Purity:
98 - 100% (HPLC)
Synonym(s):
4-(Methoxycarbonyl)benzeneboronic acid, 4-borono-benzoic acid 1-methyl ester
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Product Information

4-Methoxycarbonylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of complex organic molecules. Its unique structure allows for the introduction of functional groups, enhancing the diversity of synthesized compounds. Researchers often leverage its properties in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

In addition to its synthetic applications, 4-Methoxycarbonylphenylboronic acid exhibits potential in the field of biochemistry, particularly in the design of targeted drug delivery systems. Its boronic acid functionality can selectively bind to diols, which is beneficial in creating smart materials that respond to biological stimuli. This compound stands out due to its ease of use and compatibility with various reaction conditions, making it a preferred choice for both academic and industrial applications.

Synonyms
4-(Methoxycarbonyl)benzeneboronic acid, 4-borono-benzoic acid 1-methyl ester
CAS Number
99768-12-4
Purity
98 - 100% (HPLC)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD01632203
PubChem ID
2734369
Melting Point
240 - 250 ?C
Appearance
White powder
Conditions
Store at RT
General Information
Synonyms
4-(Methoxycarbonyl)benzeneboronic acid, 4-borono-benzoic acid 1-methyl ester
CAS Number
99768-12-4
Purity
98 - 100% (HPLC)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD01632203
PubChem ID
2734369
Melting Point
240 - 250 ?C
Appearance
White 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

4-Methoxycarbonylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, enabling researchers to create new pharmaceuticals and agrochemicals efficiently.
  • Drug Development: Its ability to form stable complexes with biomolecules makes it valuable in drug design, particularly in developing targeted therapies for various diseases.
  • Material Science: Used in the development of advanced materials, it contributes to creating polymers with enhanced properties, such as improved durability and chemical resistance.
  • Catalysis: This compound acts as a catalyst in various chemical reactions, facilitating faster and more efficient processes, which is crucial in industrial applications.
  • Analytical Chemistry: It is employed in analytical techniques to detect and quantify specific compounds, aiding researchers in environmental monitoring and quality control.

Citations