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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)-

1-methylsulfonylpiperidine-2-carboxylic acid

OC(=O)C1CCCCN1S(=O)(=O)C Request for Quotation
Chemical Name: 1-methylsulfonylpiperidine-2-carboxylic acid
CAS Number: 1008975-54-9
Product Number: AG00033O(AGN-PC-00UX85)
Synonyms:
MDL No:
Molecular Formula: C7H13NO4S
Molecular Weight: 207.2474

Identification/Properties

Computed Properties
Molecular Weight:
207.244g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
207.057g/mol
Monoisotopic Mass:
207.057g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
292
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(Methylsulfonyl)piperidine-2-carboxylic acid is a versatile compound widely used in chemical synthesis as a key building block for the creation of complex organic molecules. It serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, 1-(Methylsulfonyl)piperidine-2-carboxylic acid can be utilized as a functional group for introducing molecular diversity into target compounds. Its piperidine core provides a rigid structural framework that is often beneficial for enhancing the biological activity of the final products. Additionally, the presence of the sulfonyl group offers a handle for selective modifications, such as coupling reactions or functional group transformations.The incorporation of 1-(Methylsulfonyl)piperidine-2-carboxylic acid into synthetic pathways enables chemists to access a wide range of structurally diverse molecules with tailored properties. Its compatibility with various synthetic methods and its ability to act as a chiral pool source make it a valuable tool for organic chemists striving to design and prepare novel compounds for various applications.