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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)-

2-Pyrrolidinone, 3,3-diethyl-

CCC1(CC)CCNC1=O Request for Quotation
Chemical Name: 2-Pyrrolidinone, 3,3-diethyl-
CAS Number: 175698-05-2
Product Number: AG00AY9G(AGN-PC-0MTMBD)
Synonyms:
MDL No:
Molecular Formula: C8H15NO
Molecular Weight: 141.2108

Identification/Properties

Computed Properties
Molecular Weight:
141.214g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
141.115g/mol
Monoisotopic Mass:
141.115g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
138
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,3-Diethyl-2-pyrrolidinone, also known as DEPN, is a versatile chemical commonly used in various chemical synthesis processes. One of its key applications is as a solvent in organic reactions, thanks to its high boiling point and good solubility properties. DEPN acts as an effective medium for facilitating reactions between different compounds, allowing for increased reaction rates and improved yields.Additionally, 3,3-Diethyl-2-pyrrolidinone is utilized as a reagent in the preparation of various pharmaceuticals and agrochemicals. Its unique chemical structure enables it to participate in a range of reactions, including condensation, alkylation, and deprotonation, making it a valuable tool in the synthesis of complex molecules.Furthermore, DEPN serves as a stabilizing agent in certain chemical reactions, particularly those involving sensitive functional groups or reactive intermediates. Its ability to form stable complexes with certain compounds can help prevent side reactions and undesired byproducts, leading to cleaner and more efficient synthesis processes.