815-68-9 Usage
Uses
Used in Chemical Synthesis:
Triacetylmethane is used as a key intermediate in the synthesis of novel metal complexes, such as bis(3-acetyl-2,4-pentanedionato-O2,O3)palladium(II) and bis(3-acetyl-2,4-pentanedionato-O2,O3)magnesium(II). These metal complexes have potential applications in various fields, including catalysis, materials science, and pharmaceuticals.
Used in Organic Chemistry:
Triacetylmethane is also used in organic chemistry for the synthesis of various organic compounds. For example, its condensation with 2,6-diisopropylaniline in toluene in the presence of p-toluenesulfonic acid yields 3-[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione, which can be further utilized in the development of new organic compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 815-68-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 815-68:
(5*8)+(4*1)+(3*5)+(2*6)+(1*8)=79
79 % 10 = 9
So 815-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O3/c1-4(8)7(5(2)9)6(3)10/h8H,1-3H3
815-68-9Relevant articles and documents
Acetylation of β-diketone copper(II) chelates by treatment with ketene
Matare,Bohac,Hrnciar
, p. 381 - 382 (2007/10/02)
A new efficient method for preparation of acyclic α-acetylated β-diketone copper(II) chelates and their corresponding geminal triketones by treatment of starting β-diketone cuprates 1 with ketene is described.
O-Acylation using organothallium compounds
-
, (2008/06/13)
Thallous salts of β-dicarbonyl compounds, prepared by reaction of the β-dicarbonyl compounds with a thallous alkoxide, are treated with alkyl halides to give C-alkyl products in high yield, with acyl halides at room temperature to give C-acyl products, and with acyl halides at low temperatures to give O-acyl products. Thallous phenolates are esterified with acyl or aroyl halides. Anhydrides are also prepared, as are biaryls and bi-sec-alkyls. N-Heterocyclics, including purines and pyrimidines, are N-alkylated. Lactams are O-acylated or N-alkylated.
