Pyridine,5-bromo-2-chloro-3-iodo-


Chemical Name: Pyridine,5-bromo-2-chloro-3-iodo-
CAS Number: 928653-73-0
Product Number: AG0036XO(AGN-PC-0W1Z8V)
Synonyms:
MDL No:
Molecular Formula: C5H2BrClIN
Molecular Weight: 318.3375

Identification/Properties


Properties
BP:
397.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
318.336g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
316.81g/mol
Monoisotopic Mass:
316.81g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-BROMO-2-CHLORO-3-IODO-PYRIDINE is a versatile building block in chemical synthesis, commonly used in the production of pharmaceuticals, agrochemicals, and materials. Its unique structure with halogen substitutions enables it to participate in a variety of reactions, making it a valuable intermediate in organic synthesis.In pharmaceutical synthesis, 5-BROMO-2-CHLORO-3-IODO-PYRIDINE can be used to introduce specific functional groups and motifs into drug molecules, enhancing their potency or selectivity. Its presence can also influence the physical and chemical properties of the final compound, affecting factors such as solubility and stability.In agrochemical applications, this compound can serve as a key starting material for the synthesis of pesticides, herbicides, and fungicides. The halogen substituents on the pyridine ring can confer desirable biological activities to the resulting products, enabling targeted control of pests and pathogens in agricultural settings.Furthermore, 5-BROMO-2-CHLORO-3-IODO-PYRIDINE finds use in material science, where it can be incorporated into polymers, resins, and other materials to modify their properties. Its reactivity allows for functionalization and cross-linking reactions, leading to the development of materials with tailored properties for specific industrial applications.Overall, the strategic placement of bromine, chlorine, and iodine atoms on the pyridine ring of this compound makes it a valuable resource for chemical synthesis, offering a wide range of opportunities for the creation of diverse and specialized molecules across various sectors.