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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)-

(3S)-1-(2-chlorophenyl)-5-oxo-pyrrolidine-3-carboxylate

OC(=O)C1CC(=O)N(C1)c1ccccc1Cl Request for Quotation
Chemical Name: (3S)-1-(2-chlorophenyl)-5-oxo-pyrrolidine-3-carboxylate
CAS Number: 91349-19-8
Product Number: AG006BOE(AGN-PC-0OMMX2)
Synonyms:
MDL No:
Molecular Formula: C11H10ClNO3
Molecular Weight: 239.6550

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
239.655g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
239.035g/mol
Monoisotopic Mass:
239.035g/mol
Topological Polar Surface Area:
57.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
308
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


1-(2-Chlorophenyl)-5-oxopyrrolidine-3-carboxylic acid is a valuable compound in chemical synthesis due to its versatile applications. This compound serves as a key building block in the development of various pharmaceuticals, agricultural chemicals, and advanced materials. Its structure contains a reactive carboxylic acid group, which facilitates its involvement in a wide range of synthetic processes.In organic synthesis, 1-(2-Chlorophenyl)-5-oxopyrrolidine-3-carboxylic acid can be utilized as a precursor in the preparation of heterocyclic compounds, which are essential components in drug discovery and development. By undergoing various functional group transformations, this compound can be modified to introduce specific chemical functionalities required for the desired target molecule.Additionally, the presence of the chlorophenyl moiety in 1-(2-Chlorophenyl)-5-oxopyrrolidine-3-carboxylic acid offers opportunities for selective derivatization reactions, enabling the synthesis of novel molecular structures with potential biological activities. This compound's functionality and reactivity make it a valuable tool for synthetic chemists seeking to design and construct complex molecules for various applications in the fields of medicine, agriculture, and materials science.