Piperazine, 1-(5-bromo-2-pyridinyl)-4-methyl-


Chemical Name: Piperazine, 1-(5-bromo-2-pyridinyl)-4-methyl-
CAS Number: 364794-58-1
Product Number: AG003D1G(AGN-PC-00YV1U)
Synonyms:
MDL No:
Molecular Formula: C10H14BrN3
Molecular Weight: 256.1423

Identification/Properties


Properties
BP:
341.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
256.147g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
255.037g/mol
Monoisotopic Mass:
255.037g/mol
Topological Polar Surface Area:
19.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
180
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-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



1-(5-Bromopyridin-2-yl)-4-methylpiperazine, commonly referred to as $name$, is a versatile intermediate compound that finds extensive use in chemical synthesis processes. This compound serves as a key building block in the creation of advanced pharmaceuticals, agrochemicals, and other fine chemicals.In chemical synthesis, $name$ plays a crucial role as a functional group precursor, allowing for the introduction of specific functionalities within the molecular structure of target compounds. By leveraging the unique reactivity of the bromopyridine and piperazine moieties, chemists can modify and tailor the properties of substances for various applications.$name$ is particularly valued for its efficacy in designing novel drug candidates due to its ability to influence the biological activity, stability, and pharmacokinetic properties of the final products. Additionally, its structural characteristics enable versatile derivatization, facilitating the synthesis of diverse molecular scaffolds and complex organic compounds.Overall, the application of 1-(5-Bromopyridin-2-yl)-4-methylpiperazine in chemical synthesis underscores its significance as a valuable tool for the development of cutting-edge materials and therapeutics with enhanced performance and functionality.