793686-57-4 Usage
Description
1(2H)-Acenaphthylenone,2-methoxy-5,6-dimethyl-(9CI), also known as 1-(2-methoxy-5,6-dimethyl-1H-inden-2-yl)ethanone, is a chemical compound with the molecular formula C15H14O2. It is a ketone derivative and belongs to the class of organic compounds known as acenaphthenones. 1(2H)-Acenaphthylenone,2-methoxy-5,6-dimethyl-(9CI) is commonly used in organic synthesis and research laboratories for various purposes, including as a reagent and intermediate in the production of other chemical compounds. The specific properties and applications of this compound may vary depending on the context and the intended use.
Uses
Used in Organic Synthesis:
1(2H)-Acenaphthylenone,2-methoxy-5,6-dimethyl-(9CI) is used as a reagent in organic synthesis for the production of various chemical compounds. Its unique structure and properties make it a valuable component in the synthesis of a wide range of molecules.
Used in Research Laboratories:
1(2H)-Acenaphthylenone,2-methoxy-5,6-dimethyl-(9CI) is also used as an intermediate in research laboratories, where it can be further modified or used as a starting material for the development of new chemical entities. Its versatility and reactivity contribute to its utility in scientific research and development.
Used in Pharmaceutical Industry:
1(2H)-Acenaphthylenone,2-methoxy-5,6-dimethyl-(9CI) may also find applications in the pharmaceutical industry, where it could be used as a building block for the development of new drugs or as a component in drug delivery systems. Its specific role in this industry would depend on the target application and the desired properties of the final product.
Used in Chemical Production:
In the chemical production industry, 1(2H)-Acenaphthylenone,2-methoxy-5,6-dimethyl-(9CI) can be used as an intermediate in the manufacturing process of various chemical products. Its presence in the production chain can contribute to the development of new materials with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 793686-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,3,6,8 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 793686-57:
(8*7)+(7*9)+(6*3)+(5*6)+(4*8)+(3*6)+(2*5)+(1*7)=234
234 % 10 = 4
So 793686-57-4 is a valid CAS Registry Number.
793686-57-4Relevant articles and documents
Photolytic, thermal, addition, and cycloaddition reactions of 2-diazo-5,6- and -3,8-disubstituted acenaphthenones
Blair, Patricia A.,Chang, Sou-Jen,Shechter, Harold
, p. 7123 - 7133 (2007/10/03)
Preparation and varied thermal and photolytic reactions of 2-diazo-5,6-(disubstituted)acenaphthenones (11a-d) and 2-diazo-3,8- dimethoxyacenaphthenone (12) are reported. Alcohols react thermally and photolytically with 11a-c with losses of N2 to yield 2-alkoxynaphthenones (24a,b and 47a,b) and acenaphthenones (25 and 48a,b). Aniline and diphenylamine are converted by 11a-c at 180°C to acenaph[1,2-6]indoles (29a,b and 53a,b). Thermolyses of 11a-c at ～450°C (0.15 mmHg) yield reduction products 25 and 48a,b, respectively. Wolff rearrangements to 1,8-naphthyleneketenes (15a-d) and/or their derivatives are not observed in the above experiments. Oxygen converts 11a-c thermally to acenaphthenequinones (19a-c) and/or 1,8-naphthalic anhydrides. Insertion, addition, substitution, and/or isomerization reactions occur upon irradiation of 2-diazoacenaphthenones in cyclohexane, benzene, and tetrahydrofuran. Photolysis of 11d in benzene in the presence of O2 yields the insertion-oxidation product 2-hydroxy-5,6-dinitro-2-phenylacenaphthenone (60). Photolyses of 11a-c in nitriles result in N2 evolution and dipolar cycloaddition to give acenaph[1,2-d]oxazoles (41 and 61a,b). Acetylenes undergo thermal and photolytic cycloaddition/1,5-sigmatropic rearrangement reactions with 11a-d with N2 retention to give pyrazolo[5,1-a]quinolin-7-ones (69f-j). 2-Diazoacenaphthenones 1a and 11a react thermally and photolytically with electronegatively-substituted olefins with N2 expulsion to yield (E)- and (Z)-2-oxospiro[acenaphthylene-1(2H),1′cyclopropanes] 73a-c and 74a-c, respectively. The mechanisms of the reactions of la, 11a-d, and 12 reported are discussed.
