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Catalog Number:
40296
CAS Number:
101084-81-5
3-Carboxy-5-nitrophenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Carboxy-5-nitrobenzeneboronic acid, 3-(Dihydroxyboryl)-5-nitrobenzoic acid
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Product Information

3-Carboxy-5-nitrophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a carboxylic acid and a nitro group, making it an essential building block for the development of various pharmaceuticals and agrochemicals. Its unique structure allows for effective interactions with biological targets, enhancing its potential in drug discovery and development. Researchers often leverage its properties in the synthesis of complex molecules, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura coupling reactions.

Additionally, 3-Carboxy-5-nitrophenylboronic acid has shown promise in the field of materials science, where it can be employed in the preparation of functionalized polymers and nanomaterials. Its ability to form stable complexes with diols further expands its application in sensor technology and catalysis. With its multifunctional characteristics, this compound stands out as a valuable asset for researchers and industry professionals seeking innovative solutions in their respective fields.

Synonyms
3-Carboxy-5-nitrobenzeneboronic acid, 3-(Dihydroxyboryl)-5-nitrobenzoic acid
CAS Number
101084-81-5
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BNO6
Molecular Weight
210.94
MDL Number
MFCD00757433
PubChem ID
2773315
Melting Point
229 °C (Lit.)
Appearance
White to slightly yellow crystalline powd
Conditions
Store at RT
General Information
Synonyms
3-Carboxy-5-nitrobenzeneboronic acid, 3-(Dihydroxyboryl)-5-nitrobenzoic acid
CAS Number
101084-81-5
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BNO6
Molecular Weight
210.94
MDL Number
MFCD00757433
PubChem ID
2773315
Melting Point
229 °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

3-Carboxy-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 used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, enhancing the effectiveness of drug delivery systems.
  • Sensor Technology: The compound is applied in the creation of chemical sensors that detect specific biomolecules, aiding in diagnostics and environmental monitoring.
  • Organic Electronics: Its unique properties make it suitable for applications in organic electronics, such as organic light-emitting diodes (OLEDs), improving device efficiency.
  • Research in Catalysis: This chemical is also explored in catalytic reactions, where it can enhance reaction rates and selectivity, offering advantages over traditional catalysts.

Citations