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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-Piperidinecarbonyl chloride, 1-(methylsulfonyl)-

ClC(=O)C1CCN(CC1)S(=O)(=O)C Request for Quotation
Chemical Name: 4-Piperidinecarbonyl chloride, 1-(methylsulfonyl)-
CAS Number: 241138-40-9
Product Number: AG00BH05(AGN-PC-0NHU6Q)
Synonyms:
MDL No:
Molecular Formula: C7H12ClNO3S
Molecular Weight: 225.6931

Identification/Properties

Computed Properties
Molecular Weight:
225.687g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
225.023g/mol
Monoisotopic Mass:
225.023g/mol
Topological Polar Surface Area:
62.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
287
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methanesulfonylpiperidine-4-carbonyl chloride, also known as MSPPC, serves as a versatile reagent in chemical synthesis. This compound is commonly used as an acyl chloride derivative for introducing the 4-piperidone moiety into diverse organic molecules. In organic synthesis, MSPPC is employed for the preparation of various functionalized compounds, particularly in the pharmaceutical and agrochemical industries. Its reactivity allows for selective acylation of nucleophiles, enabling the formation of complex structures with strategic control over regioselectivity. Furthermore, the presence of the piperidine ring confers unique stereochemical properties, which can be harnessed in the design of chiral building blocks. By facilitating the introduction of the carbonyl chloride functionality, 1-methanesulfonylpiperidine-4-carbonyl chloride offers chemists a powerful tool for the elaboration of novel chemical entities with diverse biological activities.