Piperazine, 1-methyl-4-(4-piperidinyl)-


Chemical Name: Piperazine, 1-methyl-4-(4-piperidinyl)-
CAS Number: 53617-36-0
Product Number: AG003EI1(AGN-PC-0OBX7I)
Synonyms:
MDL No:
Molecular Formula: C10H21N3
Molecular Weight: 183.2938

Identification/Properties


Properties
MP:
53-56°C
BP:
260.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
183.299g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
183.174g/mol
Monoisotopic Mass:
183.174g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
146
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-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1-Methyl-4-(piperidin-4-yl)piperazine is a versatile chemical compound commonly used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structure contains both a tertiary amine and a piperazine ring, making it a crucial intermediate in the synthesis of complex organic molecules.In chemical synthesis, 1-Methyl-4-(piperidin-4-yl)piperazine acts as a key starting material for the preparation of diverse compounds. It can be functionalized at different positions to introduce specific groups or linkers, allowing chemists to tailor the structure of the final product for desired properties. The piperazine moiety in this compound provides a cyclic scaffold that imparts unique reactivity and selectivity in various reactions, making it valuable in the creation of biologically active molecules.Additionally, the presence of the methyl group and the piperidine ring in 1-Methyl-4-(piperidin-4-yl)piperazine offers opportunities for further derivatization, enabling the synthesis of analogs with enhanced properties or improved pharmacokinetic profiles. Its use in medicinal chemistry is particularly noteworthy, as it can be incorporated into drug candidates targeting a wide range of biological pathways and diseases.Overall, 1-Methyl-4-(piperidin-4-yl)piperazine plays a crucial role in chemical synthesis by serving as a versatile building block with diverse applications across various fields of chemistry. Its unique structural features and reactivity make it a valuable tool for synthesizing complex organic compounds with potential applications in pharmaceutical, agricultural, and specialty chemical industries.