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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, (2,6-dichloro-4-pyridinyl)-1-piperidinyl-

O=C(c1cc(Cl)nc(c1)Cl)N1CCCCC1 Request for Quotation
Chemical Name: Methanone, (2,6-dichloro-4-pyridinyl)-1-piperidinyl-
CAS Number: 287196-80-9
Product Number: AG002W92(AGN-PC-0KL1F6)
Synonyms:
MDL No:
Molecular Formula: C11H12Cl2N2O
Molecular Weight: 259.1318

Identification/Properties

Computed Properties
Molecular Weight:
259.13g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
258.033g/mol
Monoisotopic Mass:
258.033g/mol
Topological Polar Surface Area:
33.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
246
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


2,6-Dichloro-4-(piperidin-1-ylcarbonyl)pyridine is a valuable compound in chemical synthesis due to its versatile applications. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it an excellent intermediate for introducing both the pyridine and piperidine moieties into complex molecular structures. In medicinal chemistry, 2,6-Dichloro-4-(piperidin-1-ylcarbonyl)pyridine is often used in the development of novel drug candidates targeting a wide range of diseases. Additionally, in agrochemical synthesis, this compound plays a crucial role in the production of pesticides and herbicides. Its strategic placement of functional groups allows for efficient derivatization, enabling chemists to tailor its properties for specific applications. Overall, the versatility and reactivity of 2,6-Dichloro-4-(piperidin-1-ylcarbonyl)pyridine make it a valuable tool in the toolbox of synthetic chemists across various industries.