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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-hydroxy-1-(phenylmethyl)-, (4S)-

O[C@@H]1CN(C(=O)C1)Cc1ccccc1 Request for Quotation
Chemical Name: 2-Pyrrolidinone, 4-hydroxy-1-(phenylmethyl)-, (4S)-
CAS Number: 191403-66-4
Product Number: AG002F7C(AGN-PC-0O65VE)
Synonyms:
MDL No:
Molecular Formula: C11H13NO2
Molecular Weight: 191.2264

Identification/Properties

Computed Properties
Molecular Weight:
191.23g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
191.095g/mol
Monoisotopic Mass:
191.095g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-Benzyl-4-hydroxypyrrolidin-2-one, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties. In chemical synthesis, this compound serves as a key intermediate in the creation of various pharmaceuticals, particularly those targeting neurological disorders and mental health conditions.$name$ plays a crucial role in the development of novel drug compounds by acting as a chiral building block, enabling the synthesis of enantiopure molecules with enhanced biological activity and decreased side effects. Its chiral nature allows for the production of specific enantiomers, which are essential in drug design to ensure optimal pharmacological effects.Furthermore, $name$ is utilized in the creation of specialized ligands and catalysts for asymmetric synthesis, facilitating the production of complex molecules with high stereoselectivity. By incorporating this compound into synthetic pathways, chemists can achieve precise control over the stereochemistry of the final products, leading to more efficient and sustainable synthesis processes.Overall, the application of (S)-1-Benzyl-4-hydroxypyrrolidin-2-one in chemical synthesis contributes significantly to the advancement of pharmaceutical research and development, offering new possibilities for the design and production of biologically active compounds with potential therapeutic benefits.