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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-Piperidinamine

NC1CCNCC1 Request for Quotation
Chemical Name: 4-Piperidinamine
CAS Number: 13035-19-3
Product Number: AG003KRY(AGN-PC-0JR2FK)
Synonyms:
MDL No: MFCD02179399
Molecular Formula: C5H12N2
Molecular Weight: 100.1622

Identification/Properties

Properties
BP:
65°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Stability:
Hygroscopic
Refractive Index:
n20/D 1.4910(lit.)
Computed Properties
Molecular Weight:
100.165g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
100.1g/mol
Monoisotopic Mass:
100.1g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
48
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Piperidin-4-amine, also known as 4-aminopiperidine, is a valuable chemical building block widely used in synthetic organic chemistry. Thanks to its unique structural properties, Piperidin-4-amine serves as a versatile intermediate in various chemical reactions and synthesis pathways.One primary application of Piperidin-4-amine is its role as a key precursor in the synthesis of pharmaceutical compounds. Its cyclic amine structure makes it an essential component in the production of numerous drugs, including antiviral agents, antibiotics, and antipsychotics. By incorporating Piperidin-4-amine into molecular structures, chemists can enhance the bioactivity, stability, and selectivity of pharmaceutical products.In addition to its pharmaceutical applications, Piperidin-4-amine is also utilized in the synthesis of agrochemicals, dyes, and specialty chemicals. Its ability to participate in various chemical reactions, such as acylation, alkylation, and Mannich reactions, enables the creation of diverse organic molecules with desired properties and functions. Researchers and chemists rely on Piperidin-4-amine to introduce specific structural motifs, achieve stereochemical control, and access complex molecular architectures in the design of functional materials.Overall, Piperidin-4-amine plays a crucial role in modern chemical synthesis, facilitating the development of cutting-edge technologies, innovative materials, and life-saving medications. Its versatility and reactivity make it an indispensable tool for chemists seeking to explore new frontiers in organic chemistry and drug discovery.