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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)-

Pentanoic acid, 3-methyl-2-oxo-, calcium salt, (S)-

CC[C@@H](C(=O)C(=O)[O-])C.CC[C@@H](C(=O)C(=O)[O-])C.[Ca+2] Request for Quotation
Chemical Name: Pentanoic acid, 3-methyl-2-oxo-, calcium salt, (S)-
CAS Number: 51828-96-7
Product Number: AG00I99X(AGN-PC-0SBEUP)
Synonyms:
MDL No:
Molecular Formula: C12H18CaO6
Molecular Weight: 298.3457

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


Calcium (S)-3-methyl-2-oxopentanoate, also known as calcium methyl acetoacetate, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various reactions due to its unique properties.In chemical synthesis, Calcium (S)-3-methyl-2-oxopentanoate can act as a precursor for the preparation of numerous organic compounds. It is commonly employed as a C-C bond forming reagent in the synthesis of complex molecules. This compound can undergo condensation reactions with various nucleophiles to form β-ketoesters, which are important intermediates in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Additionally, Calcium (S)-3-methyl-2-oxopentanoate can participate in aldol condensation reactions, enabling the formation of β-hydroxyketones. These β-hydroxyketones are valuable building blocks in organic synthesis and can further undergo various transformations to yield diverse molecular structures.Furthermore, this compound can serve as a chiral source in asymmetric synthesis. The chiral center in Calcium (S)-3-methyl-2-oxopentanoate can be utilized to selectively control the stereochemistry of the products in asymmetric reactions, providing access to enantiomerically pure compounds of pharmaceutical interest.Overall, Calcium (S)-3-methyl-2-oxopentanoate is a key reagent in chemical synthesis, offering a wide range of applications in the production of complex organic molecules with precise stereochemical control.