913836-11-0

Basic information

• Product Name: 5-BORONOPICOLINIC ACID
• Synonyms: 6-CARBOXYPYRIDINE-3-BORONIC ACID;6-CARBOXY-3-PYRIDINEBORONIC ACID;5-BORONOPICOLINIC ACID;6-Carboxypyridine-3-boronic acid 97%;17 6- Carboxy pyridine -3-boronic acid;2-Carboxypyridine-5-boronic acid, 97%;5-Boronopicolinic acid, 5-Boronopyridine-2-carboxylic acid;6-Carboxypyridine-3-boronicacid97%
• CAS NO: 913836-11-0
• Molecular Formula: C6H6BNO4
• Molecular Weight: 166.92714
• Product Categories: blocks;BoronicAcids;Pyridines
• Mol File: 913836-11-0.mol
• Article Data: 0

Chemical Properties

• Melting Point: >300℃
• Boiling Point: 454.4 °C at 760 mmHg
• Flash Point: 228.6 °C
• Appearance: /
• Density: 1.5g/cm³
• Vapor Pressure: 4.78E-09mmHg at 25°C
• Refractive Index: 1.588
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 0.94±0.50(Predicted)
• CAS DataBase Reference: 5-BORONOPICOLINIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BORONOPICOLINIC ACID(913836-11-0)
• EPA Substance Registry System: 5-BORONOPICOLINIC ACID(913836-11-0)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 913836-11-0(Hazardous Substances Data)

Usage

Description

5-Boronopicolinic acid is a chemical compound that features a boron atom within its structure, along with nitrogen, carbon, and oxygen. It is a derivative of picolinic acid and is recognized for its utility in coordination chemistry as a ligand and as a precursor to a variety of functionalized materials. This versatile building block is instrumental in the synthesis of heterocyclic compounds, with its boron atom capable of engaging in diverse catalytic reactions. Its unique structure and properties render it a valuable and adaptable compound for a range of applications in the chemical and pharmaceutical sectors.

Uses

Used in Pharmaceutical Industry:
5-Boronopicolinic acid is used as a precursor in the development of new drugs, leveraging its ability to form stable complexes and its potential in catalytic reactions to enhance the properties of pharmaceutical compounds.
Used in Academic Research:
In the realm of academic research, 5-Boronopicolinic acid serves as a valuable tool for studies in organic synthesis and coordination chemistry. Its unique structural attributes and reactivity make it an essential component in advancing scientific understanding and innovation in these fields.
Used in Coordination Chemistry:
5-Boronopicolinic acid is utilized as a ligand in coordination chemistry, where it contributes to the formation of stable metal complexes. Its presence can influence the electronic properties and reactivity of these complexes, making it a key component in the design of new materials and catalysts.
Used in the Synthesis of Heterocyclic Compounds:
As a versatile building block, 5-Boronopicolinic acid is employed in the synthesis of heterocyclic compounds, which are important in various areas of chemistry, including pharmaceuticals, agrochemicals, and materials science. Its role in these syntheses is crucial for creating novel and potentially useful molecular structures.
Used in Catalytic Reactions:
The boron atom in 5-Boronopicolinic acid can participate in various catalytic reactions, making it a valuable component in processes that require the transformation of reactants into products with high selectivity and efficiency. This application is particularly relevant in the development of green chemistry processes that minimize waste and environmental impact.

InChI:InChI=1/C6H6BNO4/c9-6(10)5-2-1-4(3-8-5)7(11)12/h1-3,11-12H,(H,9,10)