609-29-0 Usage
Uses
Used in Pharmaceutical Production:
2,3-Pentanedione, 3-oxime (7CI,9CI) is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to participate in reactions that form the backbone of certain medicinal compounds, contributing to the development of new drugs and therapies.
Used in Fragrance and Flavoring Industries:
2,3-Pentanedione, 3-oxime (7CI,9CI) serves as a building block in the creation of fragrances and flavorings, adding to the complexity and variety of scents and tastes in consumer products. Its reactivity and versatility make it a valuable component in the formulation of a wide range of products, from perfumes to food additives.
Used in Organic Synthesis as a Reagent:
2,3-Pentanedione, 3-oxime (7CI,9CI) is employed as a reagent in organic synthesis, facilitating various chemical reactions that are essential in the production of a multitude of organic compounds. Its presence can enhance the efficiency of synthesis processes and enable the creation of complex molecules that are otherwise difficult to produce.
Check Digit Verification of cas no
The CAS Registry Mumber 609-29-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 609-29:
(5*6)+(4*0)+(3*9)+(2*2)+(1*9)=70
70 % 10 = 0
So 609-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2/c1-3-5(6-8)4(2)7/h8H,3H2,1-2H3/b6-5+
609-29-0Relevant academic research and scientific papers
Functionalized α-oximinoketones as building blocks for the construction of imidazoline-based potential chiral auxiliaries
Gutiérrez, Rsuini U.,Rebollar, Araceli,Bautista, Rafael,Pelayo, Vanessa,Várgas, José Luis,Montenegro, Mabel M.,Espinoza-Hicks, Carlos,Ayala, Francisco,Bernal, Pablo M.,Carrasco, Cuauhtemoc,Zepeda, L. Gerardo,Delgado, Francisco,Tamariz, Joaquín
, p. 230 - 246 (2015/03/04)
Functionalized α-oximinoketones with β-alkoxy, β-alkyl, and β-sulfenyl groups were used as efficient synthons for the preparation of chiral 1-acyl-4-imidazolin-2-ones and 1-acylimidazolidin-2-ones. For the preparation of the former heterocycles, α-oximinoketones were transformed into their respective imidazole N-oxides by neutral treatment with a chiral triazine, followed by reaction with acetic or propionic anhydrides to furnish the desired chiral 1-acetyl- or 1-propionyl-4-imidazolin-2-ones in moderate overall yields. Upon palladium hydroxide-catalyzed hydrogenation, these series were converted into their corresponding 1-acylimidazolidin-2-ones in high diastereoisomeric ratios. Thus, these novel chiral 1-acetyl- and 1-propionyl-imidazolidin-2-ones were obtained with a variety of alkyl groups at the C-4 and C-5 positions of the heterocycle, through a three-step methodology, and can be applied as new potential chiral auxiliaries.
