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Catalog Number:
40118
CAS Number:
99769-19-4
3-(Methoxycarbonyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-(Methoxycarbonyl)benzeneboronic acid
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Product Information

3-(Methoxycarbonyl)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 and industry professionals leverage its unique properties to facilitate the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its application in the development of targeted therapies highlights its significance in the pharmaceutical industry, particularly in the creation of compounds with enhanced biological activity.

Moreover, 3-(Methoxycarbonyl)phenylboronic acid serves as a valuable building block in the synthesis of various functional materials, including sensors and catalysts. Its compatibility with a range of reaction conditions and substrates allows for diverse applications, making it a preferred choice for chemists seeking efficiency and reliability in their synthetic pathways. With its proven track record in enhancing reaction yields and selectivity, this compound stands out as a crucial tool for advancing research and development in multiple fields.

Synonyms
3-(Methoxycarbonyl)benzeneboronic acid
CAS Number
99769-19-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD02093046
PubChem ID
2734714
Melting Point
209 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-(Methoxycarbonyl)benzeneboronic acid
CAS Number
99769-19-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD02093046
PubChem ID
2734714
Melting Point
209 °C (Lit.)
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-(Methoxycarbonyl)phenylboronic 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. Its ability to form stable boronate esters makes it valuable in coupling reactions.
  • Medicinal Chemistry: In drug development, it is used to create compounds that can inhibit specific biological targets. Its unique structure allows for the modification of pharmacokinetic properties, enhancing the efficacy of potential drugs.
  • Material Science: This chemical is applied in the creation of advanced materials, including polymers and nanomaterials. Its boronic acid functionality enables the formation of dynamic covalent bonds, leading to materials with tunable properties.
  • Bioconjugation: It is utilized in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules. This is particularly useful in developing biosensors and targeted drug delivery systems.
  • Environmental Applications: The compound can be used in the detection and removal of pollutants, particularly in water treatment processes. Its reactivity allows for the capture of certain contaminants, making it a useful tool in environmental chemistry.

Citations