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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-DiphenylacetoXy-N-methylpiperidine Methiodide

CN1CCC(CC1)OC(=O)C(c1ccccc1)c1ccccc1.IC Request for Quotation
Chemical Name: 4-DiphenylacetoXy-N-methylpiperidine Methiodide
CAS Number: 1952-15-4
Product Number: AG003LAR(AGN-PC-0WAFTU)
Synonyms:
MDL No:
Molecular Formula: C21H26INO2
Molecular Weight: 451.3411

Identification/Properties

Properties
MP:
202-208 °C
Storage:
Keep in dry area;2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
451.348g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
451.101g/mol
Monoisotopic Mass:
451.101g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
380
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


The 1-Methylpiperidin-4-yl 2,2-diphenylacetate compound, when paired with iodomethane in a 1:1 ratio, serves as a key reagent in chemical synthesis processes. This reaction allows for selective alkylation at the nitrogen atom of the piperidine ring, leading to the formation of novel organic compounds with diverse applications. The resulting product exhibits enhanced stability and reactivity, making it a valuable tool in the development of pharmaceuticals, agrochemicals, and materials science. Additionally, the reaction provides a convenient route for introducing functional groups and modifications in complex molecular structures, offering versatility in designing customized molecules for various industrial and research purposes.