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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)-

1-Cyclopentene-1-heptanoic acid, 5-oxo-3-[(triethylsilyl)oxy]-, methylester, (R)-

COC(=O)CCCCCCC1=C[C@@H](CC1=O)O[Si](CC)(CC)CC Request for Quotation
Chemical Name: 1-Cyclopentene-1-heptanoic acid, 5-oxo-3-[(triethylsilyl)oxy]-, methylester, (R)-
CAS Number: 118456-54-5
Product Number: AG0076CS(AGN-PC-0PBZD9)
Synonyms:
MDL No:
Molecular Formula: C19H34O4Si
Molecular Weight: 354.5564

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


(R)-Methyl 7-(5-oxo-3-((triethylsilyl)oxy)cyclopent-1-en-1-yl)heptanoate is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. In organic synthesis, this compound serves as a valuable building block for the preparation of various complex molecules. It can be utilized as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and fine chemicals.One of the key applications of (R)-Methyl 7-(5-oxo-3-((triethylsilyl)oxy)cyclopent-1-en-1-yl)heptanoate is its role as a chiral synthon in asymmetric synthesis. The chirality of the cyclopentenone moiety in the compound enables it to participate in stereoselective reactions, leading to the formation of enantiomerically pure products. This feature is particularly valuable in the synthesis of biologically active compounds where stereochemistry plays a crucial role in determining their pharmacological properties.Additionally, the presence of the triethylsilyl ether group in the molecule imparts stability and protection to reactive functional groups during synthetic transformations. This allows for selective manipulation of specific sites within the molecule without affecting the rest of the structure. This protective group strategy is commonly employed in organic synthesis to achieve complex molecular architectures efficiently.Overall, (R)-Methyl 7-(5-oxo-3-((triethylsilyl)oxy)cyclopent-1-en-1-yl)heptanoate is an essential reagent in the toolkit of synthetic chemists, enabling the construction of diverse molecular frameworks with high efficiency and control over stereochemistry.