195200-08-9 Usage
Uses
Used in Pharmaceutical Applications:
2-Azabicyclo[2.2.2]oct-5-ene-2-carboxylic acid, 7-acetyl-7-[(2,4-dinitrobenzoyl)oxy]-4,5-dimethyl-, methyl ester is used as a bioactive molecule for its potential pharmaceutical applications. The presence of the dinitrobenzoyl group suggests it may possess interesting biological activities, making it a candidate for drug development and therapeutic interventions.
Used in Materials Science:
In the field of materials science, 2-Azabicyclo[2.2.2]oct-5-ene-2-carboxylic acid, 7-acetyl-7-[(2,4-dinitrobenzoyl)oxy]-4,5-dimethyl-, methyl ester is used as a building block for the synthesis of novel polymers or more complex chemical compounds. Its unique structure allows for the creation of new materials with potentially useful properties.
Used in Chemical Synthesis:
2-Azabicyclo[2.2.2]oct-5-ene-2-carboxylic acid, 7-acetyl-7-[(2,4-dinitrobenzoyl)oxy]-4,5-dimethyl-, methyl ester is used as an intermediate in chemical synthesis processes. Its versatile structure makes it a valuable component in the preparation of a variety of advanced organic compounds for research and industrial purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 195200-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,2,0 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 195200-08:
(8*1)+(7*9)+(6*5)+(5*2)+(4*0)+(3*0)+(2*0)+(1*8)=119
119 % 10 = 9
So 195200-08-9 is a valid CAS Registry Number.
195200-08-9Relevant academic research and scientific papers
α-Acetyl- and α-Cyanovinyl 2,4-Dinitrophenyl Carboxylate as Useful Ketene Equivalents for the Diels-Alder Reaction
MaGee, David I.,Lee, May Ling
, p. 786 - 788 (2007/10/03)
Two ketene equivalents (5 and 35) have been developed for use in the Diels-Alder reaction. These dienophiles exhibit a marked increase in reactivity in comparison with the more conventional acetoxyacrylonitrile. Conversions of the cycloadducts to the requisite ketones occurs under mild, and moderate to high yielding conditions.
