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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-Benzenesulfonylpiperidine Hydrochloride

O=S(=O)(c1ccccc1)C1CCNCC1.Cl Request for Quotation
Chemical Name: 4-Benzenesulfonylpiperidine Hydrochloride
CAS Number: 1172500-91-2
Product Number: AG00HDWA(AGN-PC-0WBOEC)
Synonyms:
MDL No:
Molecular Formula: C11H16ClNO2S
Molecular Weight: 261.7682

Identification/Properties

Computed Properties
Molecular Weight:
261.764g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
261.059g/mol
Monoisotopic Mass:
261.059g/mol
Topological Polar Surface Area:
54.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
282
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Benzenesulfonylpiperidine Hydrochloride is a versatile compound widely utilized in chemical synthesis for its diverse applications. As a key intermediate in organic chemistry, this compound plays a crucial role in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical properties make it an ideal building block for the creation of complex molecules and functionalized structures.In chemical synthesis, 4-Benzenesulfonylpiperidine Hydrochloride serves as a valuable reagent for the introduction of the benzenesulfonyl group into target molecules. This functional group can act as a protecting group for amines or alcohols, facilitating selective reactions and allowing for the manipulation of molecular properties. Additionally, the piperidine moiety provides a versatile scaffold for further derivatization, enabling the synthesis of diverse chemical entities with specific functionalities.Furthermore, 4-Benzenesulfonylpiperidine Hydrochloride exhibits excellent reactivity and compatibility with a wide range of other reagents and reaction conditions. Its stability and solubility properties make it a reliable and user-friendly material for use in both academic research and industrial settings. Whether employed in the development of novel drug candidates, the production of advanced materials, or the exploration of new synthetic methodologies, this compound offers reliable performance and consistent results in various chemical synthesis applications.