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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-Piperidinepropanoic acid, 2-oxo-

OC(=O)CCN1CCCCC1=O Request for Quotation
Chemical Name: 1-Piperidinepropanoic acid, 2-oxo-
CAS Number: 117705-04-1
Product Number: AG0081G3(AGN-PC-02P8VJ)
Synonyms:
MDL No:
Molecular Formula: C8H13NO3
Molecular Weight: 171.1937

Identification/Properties

Computed Properties
Molecular Weight:
171.196g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
171.09g/mol
Monoisotopic Mass:
171.09g/mol
Topological Polar Surface Area:
57.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
191
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(2-Oxopiperidin-1-yl)propanoic acid, also known as $name$, serves as a valuable reagent in chemical synthesis due to its versatile and reactive functional groups. This compound is commonly utilized as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, $name$ can undergo a range of synthetic transformations to introduce the piperidine ring system and the carboxylic acid functionality into target molecules. Its piperidinone moiety can be further modified to access structurally diverse compounds with potential biological activities. Additionally, the presence of the carboxylic acid group in $name$ allows for the formation of amide, ester, or other types of chemical bonds, enabling the construction of complex molecular architectures. Overall, the strategic incorporation of 3-(2-Oxopiperidin-1-yl)propanoic acid in chemical reactions provides chemists with a powerful tool for the construction of novel molecules with desired properties.