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Catalog Number:
40305
CAS Number:
80500-28-3
4-Carboxy-3-nitrophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
4-Carboxy-3-nitrobenzeneboronic acid
Documents
$75.11 /200MG
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Product Information

4-Carboxy-3-nitrophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique properties allow it to serve as a building block in the synthesis of biologically active molecules, including potential anti-cancer agents and other therapeutic compounds. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, which are pivotal in creating complex organic structures efficiently.

Additionally, 4-Carboxy-3-nitrophenylboronic acid is recognized for its application in sensor technology, particularly in the detection of sugars and other biomolecules due to its selective binding capabilities. Its stability and reactivity make it a preferred choice for chemists looking to enhance the efficiency of their synthetic pathways while minimizing by-product formation. The compound's ability to facilitate the development of innovative materials further underscores its significance in both academic and industrial settings.

Synonyms
4-Carboxy-3-nitrobenzeneboronic acid
CAS Number
80500-28-3
Purity
98 - 105% (Assay by titration)
Molecular Formula
C7H6BNO6
Molecular Weight
210.94
MDL Number
MFCD10696661
PubChem ID
329047
Melting Point
220 °C (Lit.)
Appearance
White to slightly yellow crystalline powd
Conditions
Store at RT
General Information
Synonyms
4-Carboxy-3-nitrobenzeneboronic acid
CAS Number
80500-28-3
Purity
98 - 105% (Assay by titration)
Molecular Formula
C7H6BNO6
Molecular Weight
210.94
MDL Number
MFCD10696661
PubChem ID
329047
Melting Point
220 °C (Lit.)
Appearance
White to slightly yellow crystalline powd
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-Carboxy-3-nitrophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies that utilize boron-containing compounds for enhanced efficacy.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital in creating targeted drug delivery systems and diagnostic tools.
  • Organic Electronics: The compound plays a significant role in the fabrication of organic electronic devices, such as organic light-emitting diodes (OLEDs), due to its unique electronic properties that enhance device performance.
  • Environmental Monitoring: It is used in the development of sensors for detecting environmental pollutants, particularly in water quality testing, where its sensitivity to specific contaminants is advantageous.
  • Chemical Research: This compound is valuable in synthetic organic chemistry for creating complex molecules, providing a versatile tool for researchers looking to explore new chemical pathways and reactions.

Citations