1-methylpiperidine-4-sulfonamide


Chemical Name: 1-methylpiperidine-4-sulfonamide
CAS Number: 929632-63-3
Product Number: AG00IHF0(AGN-PC-0WD8CT)
Synonyms:
MDL No: MFCD16671952
Molecular Formula: C6H14N2O2S
Molecular Weight: 178.2526

Identification/Properties


Computed Properties
Molecular Weight:
178.25g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
178.078g/mol
Monoisotopic Mass:
178.078g/mol
Topological Polar Surface Area:
71.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
211
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

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NMR Spectrum


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Chemical Structure



1-Methylpiperidine-4-sulfonamide, also known as $name$, is a versatile compound widely used in chemical synthesis processes. In organic chemistry, this compound serves as a valuable intermediate for the synthesis of various pharmaceuticals, agrochemicals, and functional materials.Its unique structural properties, including the presence of a sulfonamide group and a piperidine ring, make it a key building block in the production of biologically active compounds. The sulfonamide group can participate in a range of important reactions, such as nucleophilic substitutions and metal-catalyzed transformations, offering chemists multiple ways to modify and functionalize the molecule.One of the primary applications of 1-Methylpiperidine-4-sulfonamide is in the construction of heterocyclic structures, which are common motifs found in many natural products and drugs. By incorporating this compound into synthetic pathways, chemists can efficiently access complex molecules with specific pharmacological or biological activities.Moreover, 1-Methylpiperidine-4-sulfonamide's compatibility with various reaction conditions and its ability to act as a chiral auxiliary further enhance its utility in chemical synthesis. Whether used for asymmetric transformations or as a protecting group strategy, this compound offers chemists a versatile tool for controlling stereochemistry and regioselectivity in their target molecule.Overall, 1-Methylpiperidine-4-sulfonamide plays a crucial role in the synthesis of diverse chemical compounds, making it an essential component in the toolkit of synthetic chemists striving to create novel molecules with tailored properties and functions.