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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)-

3-Pyrrolidinecarboxylic acid, 5-oxo-1-(2-pyridinylmethyl)-

OC(=O)C1CC(=O)N(C1)Cc1ccccn1 Request for Quotation
Chemical Name: 3-Pyrrolidinecarboxylic acid, 5-oxo-1-(2-pyridinylmethyl)-
CAS Number: 845546-25-0
Product Number: AG008HMK(AGN-PC-0LH5BN)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O3
Molecular Weight: 220.2246

Identification/Properties

Computed Properties
Molecular Weight:
220.228g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
220.085g/mol
Monoisotopic Mass:
220.085g/mol
Topological Polar Surface Area:
70.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
293
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chemical compound 5-Oxo-1-(pyridin-2-ylmethyl)pyrrolidine-3-carboxylic acid, also known as $name$, is widely utilized in chemical synthesis as a versatile building block. Its unique structure offers a range of functional groups that enable it to participate in various reactions and transformations, making it an invaluable tool for creating complex organic molecules. In particular, $name$ is frequently employed in the formation of heterocyclic compounds and pharmaceutical intermediates due to its ability to engage in diverse bond-forming processes. Its presence in the synthesis of such compounds highlights its significance in the advancement of drug discovery and material science.