856848-33-4

Basic information

• Product Name: 2-Amino-4,5-dibromopyridine
• Synonyms: 2-Amino-4,5-dibromopyridine;4,5-DibroMopyridin-2-aMine;4,5-Dibromo-pyridin-2-ylamine
• CAS NO: 856848-33-4
• Molecular Formula: C5H4Br2N2
• Molecular Weight: 251.90666
• Mol File: 856848-33-4.mol

Chemical Properties

• Melting Point: 145-145.5 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 293.9±35.0 °C(Predicted)
• Appearance: /
• Density: 2.147±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 3.61±0.24(Predicted)
• CAS DataBase Reference: 2-Amino-4,5-dibromopyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-4,5-dibromopyridine(856848-33-4)
• EPA Substance Registry System: 2-Amino-4,5-dibromopyridine(856848-33-4)

Safety Data

• Hazardous Substances Data: 856848-33-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-Amino-4,5-dibromopyridine is utilized as a key building block in organic synthesis for the creation of various biologically active molecules. Its presence of bromine atoms and an amino group allows for versatile chemical reactions, facilitating the development of new compounds with potential applications across different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Amino-4,5-dibromopyridine is employed as a precursor in the development of new drugs. Its unique structure contributes to the design of molecules with specific pharmacological properties, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemical Development:
2-Amino-4,5-dibromopyridine also finds application in the agrochemical sector, where it serves as a starting material for the synthesis of new agrochemicals. Its reactivity and structural features are harnessed to produce compounds with potential agricultural applications, such as pesticides or herbicides, aiming to enhance crop protection and yield.
Overall, 2-Amino-4,5-dibromopyridine is a versatile and promising compound with a wide range of applications in organic synthesis, pharmaceutical research, and agrochemical development, owing to its distinctive chemical properties and reactivity.