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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)-

Cyclopentanone, 3-phenyl-, (3R)-

O=C1CC[C@H](C1)c1ccccc1 Request for Quotation
Chemical Name: Cyclopentanone, 3-phenyl-, (3R)-
CAS Number: 86505-44-4
Product Number: AG003C9S(AGN-PC-0OKFDN)
Synonyms:
MDL No:
Molecular Formula: C11H12O
Molecular Weight: 160.21238

Identification/Properties

Properties
BP:
276.102°C at 760 mmHg
Computed Properties
Molecular Weight:
160.216g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
160.089g/mol
Monoisotopic Mass:
160.089g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
168
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-3-Phenylcyclopentanone is a valuable chiral building block commonly employed in chemical synthesis. Its unique structure, consisting of a cyclopentanone ring with a phenyl group attached, makes it a versatile intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, (R)-3-Phenylcyclopentanone serves as a key starting material for the asymmetric synthesis of chiral compounds. Its chiral nature allows for the creation of enantiomerically pure molecules, which are crucial in drug discovery and development. By utilizing (R)-3-Phenylcyclopentanone as a chiral template, chemists can efficiently access a wide range of structurally complex and biologically active molecules.Moreover, the presence of the phenyl group in (R)-3-Phenylcyclopentanone provides opportunities for further derivatization through various functional group transformations. This flexibility allows for the introduction of different chemical motifs, enabling the synthesis of diverse compounds with tailored properties.Overall, the application of (R)-3-Phenylcyclopentanone in chemical synthesis offers a powerful tool for accessing enantiopure compounds and structurally diverse molecules with potential applications across different industries.