4-Piperidinamine, 1-methyl-N-(1-methyl-4-piperidinyl)-


Chemical Name: 4-Piperidinamine, 1-methyl-N-(1-methyl-4-piperidinyl)-
CAS Number: 117927-28-3
Product Number: AG008RQX(AGN-PC-0KKOFY)
Synonyms:
MDL No:
Molecular Formula: C12H25N3
Molecular Weight: 211.3470

Identification/Properties


Computed Properties
Molecular Weight:
211.353g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
211.205g/mol
Monoisotopic Mass:
211.205g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
159
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

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NMR Spectrum


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Chemical Structure



1-Piperidinamine, 4-methyl-N-(1-methyl-4-piperidinyl)- is a versatile chemical compound that finds wide application in chemical synthesis processes. Due to its unique structure and properties, this compound is commonly used as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its presence allows for the synthesis of complex molecules by serving as a building block or a precursor in multistep synthesis routes.In the field of medicinal chemistry, 1-Piperidinamine, 4-methyl-N-(1-methyl-4-piperidinyl)- plays a crucial role in the development of novel drug candidates. Its incorporation into drug molecules can lead to modifications in their pharmacokinetic and pharmacodynamic profiles, enhancing their biological activity or improving their solubility and stability. Additionally, this compound can be utilized to introduce specific functional groups or chiral centers into the target molecules, influencing their interactions with biological targets and potential therapeutic effects.Moreover, in the realm of agrochemical synthesis, 1-Piperidinamine, 4-methyl-N-(1-methyl-4-piperidinyl)- serves as a valuable building block for the creation of pesticides, herbicides, and fungicides. Its inclusion in the molecular structure of these agricultural chemicals can impart desirable properties such as increased potency, selectivity, or environmental stability.Overall, the strategic use of 1-Piperidinamine, 4-methyl-N-(1-methyl-4-piperidinyl)- in chemical synthesis enables the efficient construction of diverse molecules with tailored properties for applications in pharmaceuticals, agrochemicals, and other industries.