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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, 4-[3-(cyclopentyloxy)-4-methoxyphenyl]-, (4S)-

COc1ccc(cc1OC1CCCC1)[C@H]1CNC(=O)C1 Request for Quotation
Chemical Name: 2-Pyrrolidinone, 4-[3-(cyclopentyloxy)-4-methoxyphenyl]-, (4S)-
CAS Number: 85416-73-5
Product Number: AG008F4J(AGN-PC-0OJWOX)
Synonyms:
MDL No:
Molecular Formula: C16H21NO3
Molecular Weight: 275.3428

Identification/Properties

Computed Properties
Molecular Weight:
275.348g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
275.152g/mol
Monoisotopic Mass:
275.152g/mol
Topological Polar Surface Area:
47.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
341
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chiral compound (S)-4-(3-(Cyclopentyloxy)-4-methoxyphenyl)pyrrolidin-2-one plays a crucial role in chemical synthesis, particularly in the field of asymmetric synthesis. With its unique structure and stereochemistry, this compound serves as a valuable building block for the creation of pharmaceuticals, agrochemicals, and other fine chemicals. Its presence in a variety of synthetic pathways allows for the formation of intricate molecular structures with high levels of stereoselectivity, enabling chemists to access specific enantiomers with precision. In addition, the functional groups present in this compound offer opportunities for further derivatization, expanding the scope of its applications in the synthesis of diverse chemical compounds. The (S)-4-(3-(Cyclopentyloxy)-4-methoxyphenyl)pyrrolidin-2-one stands as a versatile tool in the hands of synthetic chemists, facilitating the construction of complex molecules with exceptional control over stereochemistry and functionality.