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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-METHYLPIPERIDINO)(4-PIPERIDINYL)METHANONE HYDROCHLORIDE

CC1CCN(CC1)C(=O)C1CCNCC1.Cl Request for Quotation
Chemical Name: (4-METHYLPIPERIDINO)(4-PIPERIDINYL)METHANONE HYDROCHLORIDE
CAS Number: 690632-27-0
Product Number: AG005YF5(AGN-PC-0KL71E)
Synonyms:
MDL No:
Molecular Formula: C12H23ClN2O
Molecular Weight: 246.7768

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
246.779g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
246.15g/mol
Monoisotopic Mass:
246.15g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
216
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (4-Methylpiperidin-1-yl)(piperidin-4-yl)methanone hydrochloride, also known as $name$, serves as a versatile reagent in chemical synthesis. This unique compound is utilized as a key intermediate in numerous organic transformations and reactions. Its strategic placement of functional groups allows for selective modifications while maintaining overall molecular integrity. In organic synthesis, $name$ plays a crucial role as a building block for the construction of complex molecules with tailored properties. Its application extends to the creation of pharmaceuticals, agrochemicals, and materials with specific functions. Additionally, the controlled use of $name$ enables chemists to explore new synthetic pathways and enhance the efficiency of multi-step syntheses.