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Catalog Number:
40218
CAS Number:
117342-20-8
3-(Methoxycarbonyl)-5-nitrophenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-(Methoxycarbonyl)-5-nitrobenzeneboronic acid
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Product Information

3-(Methoxycarbonyl)-5-nitrophenylboronic acid is a versatile boronic acid derivative that plays a significant 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 the development of various pharmaceutical agents and agrochemicals. Its unique structure allows for selective reactions, which can be particularly beneficial in the synthesis of complex molecules, including those used in drug discovery and development. Researchers appreciate its utility in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing carbon-carbon bonds, thereby facilitating the creation of diverse organic compounds.

Moreover, 3-(Methoxycarbonyl)-5-nitrophenylboronic acid exhibits potential applications in the field of materials science, particularly in the development of sensors and catalysts. Its ability to interact with biological molecules opens avenues for research in targeted drug delivery systems. The compound's stability and reactivity make it a valuable tool for chemists looking to innovate in synthetic methodologies. With its broad range of applications, this boronic acid derivative stands out as a crucial component for professionals aiming to enhance their research and development projects.

Synonyms
3-(Methoxycarbonyl)-5-nitrobenzeneboronic acid
CAS Number
117342-20-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H8BNO6
Molecular Weight
224.96
MDL Number
MFCD02179469
PubChem ID
2773492
Melting Point
224 °C (Lit.)
Appearance
White to off white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-(Methoxycarbonyl)-5-nitrobenzeneboronic acid
CAS Number
117342-20-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H8BNO6
Molecular Weight
224.96
MDL Number
MFCD02179469
PubChem ID
2773492
Melting Point
224 °C (Lit.)
Appearance
White to off white 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)-5-nitrophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted therapies for cancer treatment.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostic tools.
  • Organic Synthesis: The compound is used in organic synthesis as a versatile building block for creating complex organic molecules, which is essential in materials science and polymer chemistry.
  • Sensor Technology: It finds application in the development of chemical sensors, particularly for detecting specific analytes in environmental monitoring and food safety.
  • Research in Catalysis: This chemical is utilized in catalysis research, where it helps in the development of new catalytic systems that can improve reaction efficiency and selectivity.

Citations