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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-, methyl ester

COC(=O)C1CNC(=O)C1 Request for Quotation
Chemical Name: 3-Pyrrolidinecarboxylic acid, 5-oxo-, methyl ester
CAS Number: 35309-35-4
Product Number: AG003586(AGN-PC-00KZAY)
Synonyms:
MDL No: MFCD08275678
Molecular Formula: C6H9NO3
Molecular Weight: 143.1406

Identification/Properties

Properties
MP:
62 - 64 °C
BP:
135 - 138 °C at 1 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.465
Computed Properties
Molecular Weight:
143.142g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
143.058g/mol
Monoisotopic Mass:
143.058g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
166
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


Methyl 5-Oxopyrrolidine-3-carboxylate is a valuable building block in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a versatile intermediate, offering a range of applications in the creation of pharmaceuticals, agrochemicals, and various fine chemicals.One of the key uses of Methyl 5-Oxopyrrolidine-3-carboxylate is in the synthesis of heterocyclic compounds. By reacting this compound with a variety of functional groups, chemists are able to construct complex ring structures that are crucial in the development of bioactive molecules. Additionally, the presence of the ester and ketone functionalities in Methyl 5-Oxopyrrolidine-3-carboxylate provides opportunities for further derivatization, allowing for the introduction of different chemical moieties to tailor the properties of the final product.Moreover, Methyl 5-Oxopyrrolidine-3-carboxylate can participate in various types of reactions, such as nucleophilic additions, condensations, and cyclizations, making it a versatile starting material for the synthesis of diverse organic compounds. Its ability to undergo selective transformations under specific reaction conditions makes it a valuable asset in the hands of synthetic chemists striving to access new molecules for research and development purposes.