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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(3H)-Furanone, 4-(fluoromethyl)dihydro-, (4S)-

FC[C@@H]1COC(=O)C1 Request for Quotation
Chemical Name: 2(3H)-Furanone, 4-(fluoromethyl)dihydro-, (4S)-
CAS Number: 916069-80-2
Product Number: AG01EE3G(AGN-PC-0OMRZC)
Synonyms:
MDL No:
Molecular Formula: C5H7FO2
Molecular Weight: 118.1062832

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-4-(Fluoromethyl)dihydrofuran-2(3H)-one is a versatile compound that finds wide applications in chemical synthesis, particularly in the field of organic chemistry. Its unique structural properties make it a valuable building block in the synthesis of complex molecules and pharmaceutical compounds.One of the key applications of (S)-4-(Fluoromethyl)dihydrofuran-2(3H)-one is as a chiral starting material for the asymmetric synthesis of various biologically active molecules. Its chirality plays a crucial role in controlling the stereochemistry of the final products, making it an important tool for the preparation of enantiomerically pure compounds.Additionally, (S)-4-(Fluoromethyl)dihydrofuran-2(3H)-one can be used as a substrate in cross-coupling reactions, allowing for the introduction of fluoromethyl groups into organic molecules. This functional group is valuable in medicinal chemistry and agrochemical research, as fluorinated compounds often exhibit enhanced biological activities and improved properties.Furthermore, the presence of the dihydrofuran ring in (S)-4-(Fluoromethyl)dihydrofuran-2(3H)-one provides a unique reactivity profile, enabling the construction of complex molecular frameworks through cycloaddition and ring-closing reactions. This versatility makes it a valuable intermediate in the synthesis of natural products and pharmaceuticals with diverse structural motifs.In conclusion, (S)-4-(Fluoromethyl)dihydrofuran-2(3H)-one is a valuable compound in chemical synthesis, offering synthetic chemists a powerful tool for the creation of structurally diverse molecules with applications in various fields of chemistry.