69225-59-8 Usage
Description
1,4-Cyclohexanedione mono(2,2-dimethyltrimethylene ketal) is an organic compound characterized by its white to yellowish powder form. It is a derivative of cyclohexanedione with a unique ketal functional group, which contributes to its specific chemical properties and reactivity.
Uses
Used in Chemical Synthesis:
1,4-Cyclohexanedione mono(2,2-dimethyltrimethylene ketal) is used as a reagent for the preparation of carbazole derivatives. Its unique structure allows it to participate in various chemical reactions, facilitating the synthesis of complex organic molecules, particularly those with potential applications in pharmaceuticals, materials science, and other industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,4-Cyclohexanedione mono(2,2-dimethyltrimethylene ketal) may be utilized as a key intermediate in the synthesis of certain drugs or drug candidates. Its ability to form carbazole derivatives can be particularly valuable in the development of novel therapeutic agents.
Used in Materials Science:
1,4-Cyclohexanedione mono(2,2-dimethyltrimethylene ketal) may also find applications in the field of materials science, where its chemical properties can be exploited to create new materials with specific characteristics. These materials could have potential uses in various industries, such as electronics, coatings, or adhesives.
Synthesis Reference(s)
Synthetic Communications, 14, p. 39, 1984 DOI: 10.1080/00397918408060862
Check Digit Verification of cas no
The CAS Registry Mumber 69225-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69225-59:
(7*6)+(6*9)+(5*2)+(4*2)+(3*5)+(2*5)+(1*9)=148
148 % 10 = 8
So 69225-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O3/c1-10(2)7-13-11(14-8-10)5-3-9(12)4-6-11/h3-8H2,1-2H3
69225-59-8Relevant articles and documents
AN IMPROVED PROCESS FOR THE PREPARATION OF FROVATRIPTAN
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Page/Page column 14-15, (2012/11/13)
A process for the preparation and purification of Frovatriptan of formula (I) and its enantiomers, particuariy the R- enantiomer is disclosed, comprising formation of the di-p-toluoyltartaric acid salt of Frovatriptan.
METHOD FOR PRODUCING CARBONYL COMPOUND AN PRO-OXIDANT USED FOR PRODUCTION OF CARBONYL COMPOUND
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Page/Page column 12; 14-15, (2009/08/16)
The invention provides a process for the preparation of a carbonyl compound in high efficiency by oxidizing an alcohol. The process for the preparation of a carbonyl compound of the present invention includes a step of oxidizing an alcohol in the presence of a compound of the formula (I) or a derivative or a salt thereof, and an oxidant, wherein R1 and R2 independently represent hydrogen, a halogen, a nitro or acidic group, or an alkyl or alkoxy group, each of which optionally has a substituent, or R1 and R2 combine the two carbon atoms to which they are boned to form an aromatic ring.
A new efficient deprotection of azines, hydrazones and oximes. An excellent route for exchanging oxygen isotopes in carbonyls
Carmeli, Mira,Rozen, Shlomo
, p. 763 - 766 (2007/10/03)
Carbonyls, protected as azines or other C=N derivatives can be deprotected by HOF·CH3CN in seconds to the corresponding ketone or aldehyde in very good yields. This reaction also offers a very efficient route for replacing the oxygen atom of most carbonyls with any other oxygen isotope, for example, [18]O.