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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)-

Methanone, phenyl-4-piperidinyl-, hydrochloride

O=C(c1ccccc1)C1CCNCC1.Cl Request for Quotation
Chemical Name: Methanone, phenyl-4-piperidinyl-, hydrochloride
CAS Number: 25519-80-6
Product Number: AG003TPH(AGN-PC-0KK0AA)
Synonyms:
MDL No:
Molecular Formula: C12H16ClNO
Molecular Weight: 225.7145

Identification/Properties

Properties
MP:
223-225°C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
225.716g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
225.092g/mol
Monoisotopic Mass:
225.092g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
191
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phenyl(piperidin-4-yl)methanone hydrochloride is a versatile compound commonly used in chemical synthesis due to its unique properties. Its application in organic chemistry includes acting as a key intermediate in the production of various pharmaceuticals, specifically those related to central nervous system disorders. This compound serves as a valuable building block in the synthesis of complex molecules with biological activity. Additionally, it is utilized in research settings for the development of new drugs and medicinal compounds. Its selective reactivity and functional groups make it an essential component in the creation of innovative chemical structures with potential therapeutic applications.