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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, 4-oxo-, ethyl ester, hydrochloride (1:1)

CCOC(=O)C1CNCC1=O.Cl Request for Quotation
Chemical Name: 3-Pyrrolidinecarboxylic acid, 4-oxo-, ethyl ester, hydrochloride (1:1)
CAS Number: 916814-29-4
Product Number: AG0036SV(AGN-PC-0J0Y7O)
Synonyms:
MDL No:
Molecular Formula: C7H12ClNO3
Molecular Weight: 193.6281

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
193.627g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
193.051g/mol
Monoisotopic Mass:
193.051g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
179
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 4-oxopyrrolidine-3-carboxylate hydrochloride is a versatile compound commonly used in chemical synthesis. It serves as a crucial building block in the production of pharmaceuticals, agrochemicals, and various other fine chemicals. This particular compound offers valuable functionality in synthetic processes due to its unique structure and reactivity. Its incorporation into complex molecules allows for the formation of intricate chemical structures, often essential for the development of new compounds with specific properties and functions.Ethyl 4-oxopyrrolidine-3-carboxylate hydrochloride is particularly favored in the pharmaceutical industry for its role in the synthesis of bioactive compounds, including drugs and therapeutic agents. Its presence in the chemical synthesis process enables the creation of novel drug candidates with potentially improved efficacy and reduced side effects.Furthermore, this compound exhibits compatibility with a wide range of other reagents and building blocks, making it a versatile and reliable component in various synthetic routes. Its ability to undergo diverse chemical transformations enhances its utility in the creation of structurally diverse and biologically relevant molecules.Overall, Ethyl 4-oxopyrrolidine-3-carboxylate hydrochloride plays a crucial role in advancing chemical synthesis capabilities, particularly in the realm of drug discovery and development. Its versatility, reactivity, and strategic placement within synthetic pathways make it an indispensable tool for chemists striving to create innovative and valuable compounds.