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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)-

N-piperidin-3-ylmethanesulfonamide

CS(=O)(=O)NC1CCCNC1 Request for Quotation
Chemical Name: N-piperidin-3-ylmethanesulfonamide
CAS Number: 944068-21-7
Product Number: AG003SB8(AGN-PC-02MQAQ)
Synonyms:
MDL No: MFCD09810664
Molecular Formula: C6H14N2O2S
Molecular Weight: 178.2526

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
178.25g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
178.078g/mol
Monoisotopic Mass:
178.078g/mol
Topological Polar Surface Area:
66.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
207
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(3-Piperidyl)methanesulfonamide is a versatile compound widely used in chemical synthesis for its valuable applications. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, N-(3-Piperidyl)methanesulfonamide is utilized as a derivatizing agent to introduce specific functional groups or to protect reactive sites in organic molecules, facilitating selective transformations and enhancing the overall synthetic process efficiency. Its unique combination of a piperidine ring and a methanesulfonamide group enables it to participate in diverse chemical reactions, such as nucleophilic substitutions, acylations, and cyclizations, leading to the formation of complex molecular structures with high precision and control.Furthermore, N-(3-Piperidyl)methanesulfonamide plays a crucial role in the development of novel drug candidates and bioactive compounds by serving as a key component in the synthesis of heterocyclic compounds and pharmacophores. Its ability to modulate biological activity and enhance drug-like properties makes it a valuable asset in medicinal chemistry and drug discovery research.Overall, the application of N-(3-Piperidyl)methanesulfonamide in chemical synthesis is essential for expanding the capabilities of organic chemists in designing and creating intricate molecular architectures with diverse functionalities and applications.