Intermediates

3-Bromoisonicotinic Acid

  • CAS No.13959-02-9
  • GradeIndustrial / Pharmaceutical
  • Availability● In Stock

High-purity 3-Bromoisonicotinic Acid (CAS 13959-02-9) supplied for advanced organic synthesis. Reliable quality with ≥98.0% assay for pharmaceutical research.

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Product Technical Details

Product Overview

3-Bromoisonicotinic Acid is a highly specialized heterocyclic compound that serves as a fundamental building block in modern medicinal chemistry and advanced organic synthesis. Characterized by its pyridine ring structure substituted with a bromine atom at the three-position and a carboxylic acid group at the four-position, this molecule offers unique reactivity profiles essential for complex chemical transformations. Our facility produces this compound under stringent quality control standards to ensure consistency and reliability for research and industrial applications.

The structural integrity of this brominated pyridine derivative allows for versatile functionalization, making it a preferred choice for chemists designing novel pharmaceutical agents agrochemicals and functional materials. The bromine substituent acts as an excellent leaving group for various cross-coupling reactions while the carboxylic acid moiety provides opportunities for amidation or esterification. This dual functionality significantly enhances its utility in multi-step synthesis routes.

Technical Specifications

ParameterValue
Chemical Name3-Bromoisonicotinic Acid
CAS Number13959-02-9
Molecular FormulaC6H4BrNO2
Molecular Weight202.005
AppearanceOff-white crystalline powder
Assay≥98.0%
Melting Point237-238°C
Boiling Point403.1±30.0°C at 760 mmHg
Density1.8±0.1 g/cm3

Industrial Applications

This compound serves as a critical building block in the synthesis of various pharmacologically active substances. It is extensively utilized in the development of kinase inhibitors and other therapeutic candidates where the pyridine scaffold is required for biological activity. The high purity grade we supply ensures minimal impurity interference during sensitive catalytic processes which is vital for maintaining reaction efficiency and yield.

Common reactions involving this material include Suzuki-Miyaura cross-coupling Buchwald-Hartwig amination and nucleophilic aromatic substitution. These transformations enable the construction of complex biaryl systems and nitrogen-containing heterocycles found in many modern drug candidates. Additionally it finds application in the preparation of ligands for coordination chemistry and materials science research where specific electronic properties are needed.

Quality Assurance and Handling

Our manufacturing facility adheres to strict quality management systems to guarantee that every batch meets the specified assay requirements. Each production lot undergoes comprehensive analysis using high-performance liquid chromatography and nuclear magnetic resonance spectroscopy to verify identity and purity. A Certificate of Analysis is provided with every shipment to support your regulatory documentation and quality assurance protocols.

Proper storage involves keeping the material in a cool ventilated place away from incompatible substances such as strong oxidizing agents. The product is typically packaged in 25 kg drums but custom packaging solutions are available to meet specific logistical requirements. We recommend handling this chemical with appropriate personal protective equipment including gloves and safety goggles to ensure laboratory safety during weighing and transfer operations.