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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-Pyrimidinamine, 6-(1-piperidinyl)-

Nc1ncnc(c1)N1CCCCC1 Request for Quotation
Chemical Name: 4-Pyrimidinamine, 6-(1-piperidinyl)-
CAS Number: 69206-89-9
Product Number: AG00FE9D(AGN-PC-0NJ1T4)
Synonyms:
MDL No:
Molecular Formula: C9H14N4
Molecular Weight: 178.2343

Identification/Properties

Computed Properties
Molecular Weight:
178.239g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
178.122g/mol
Monoisotopic Mass:
178.122g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
156
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(Piperidin-1-yl)pyrimidin-4-amine, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ plays a crucial role as a key intermediate in the production of heterocyclic compounds. Its functional groups and structural features make it an ideal starting material for the synthesis of complex molecules with desired biological or physical properties. By utilizing $name$ as a substrate, chemists can introduce different substituents or modify its structure to create novel compounds with specific functions.One of the prominent applications of 6-(Piperidin-1-yl)pyrimidin-4-amine is in the development of potential drug candidates. Its presence in the molecular structure of pharmaceuticals can enhance the bioactivity, stability, or solubility of the final product. Additionally, the versatility of $name$ allows for the synthesis of diverse analogs and derivatives, enabling structure-activity relationship studies and optimization of drug properties.Moreover, in the field of materials science, 6-(Piperidin-1-yl)pyrimidin-4-amine is utilized for the construction of advanced polymer systems, functional coatings, or molecular probes. Its ability to participate in various chemical reactions and form intricate molecular architectures makes it a valuable component in the design of innovative materials with tailored properties.Overall, the versatile nature and utility of 6-(Piperidin-1-yl)pyrimidin-4-amine make it a valuable tool in chemical synthesis, enabling the creation of diverse compounds with applications across different sectors of the chemical industry.