Pyridine, 2,6-dibromo-3,5-dimethyl-


Chemical Name: Pyridine, 2,6-dibromo-3,5-dimethyl-
CAS Number: 117846-58-9
Product Number: AG0033JI(AGN-PC-0JWHWH)
Synonyms:
MDL No:
Molecular Formula: C7H7Br2N
Molecular Weight: 264.9452

Identification/Properties


Properties
BP:
303.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
264.948g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
264.892g/mol
Monoisotopic Mass:
262.895g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
106
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



3,5-Dimethyl-2,6-dibromopyridine is a versatile building block in chemical synthesis, commonly used as a reagent in various organic reactions. Its unique structure and properties make it particularly valuable in the field of organic chemistry.One of the primary applications of 3,5-Dimethyl-2,6-dibromopyridine is in the synthesis of biologically active compounds and pharmaceuticals. Its bromine functional groups can undergo substitution reactions, allowing for the introduction of different substituents onto the pyridine ring. This enables chemists to modify the molecule to create new drug candidates or intermediates for further synthesis.Additionally, 3,5-Dimethyl-2,6-dibromopyridine is widely employed in the preparation of coordination complexes and organometallic compounds. Its ability to coordinate with transition metals makes it a valuable ligand in catalytic processes and metal-mediated reactions. By tuning the electronic and steric properties of the molecule, chemists can control the reactivity and selectivity of metal-catalyzed transformations.Furthermore, this compound is often used in material science for the synthesis of polymers, dendrimers, and other advanced materials. Its aromatic nature and halogen substituents can facilitate polymerization reactions and cross-coupling processes, leading to the development of novel polymeric materials with tailored properties.Overall, 3,5-Dimethyl-2,6-dibromopyridine plays a crucial role in modern chemical synthesis, enabling chemists to access a wide range of compounds with diverse applications in pharmaceuticals, catalysis, and materials science.