5507-27-7 Usage
Derivative of butanedioic acid
Modified version of the parent compound butanedioic acid.
Benzylidene group
A central phenyl ring with a carbon-carbon double bond.
Methoxy substituents
Two -OCH3 groups attached to the phenyl ring in ortho positions (adjacent to each other).
Organic synthesis applications
Can be used as a building block for creating more complex organic molecules.
Medicinal chemistry potential
Possesses properties that may lead to the development of new drugs and therapeutic agents.
Pharmacologically active molecules
Can be synthesized into compounds with potential effects on biological systems.
Biological activity
May exhibit interactions with living organisms, warranting further study for potential applications.
Chemical properties
Characteristics that influence its reactivity and behavior in chemical reactions.
Reactivity
The compound's tendency to undergo chemical reactions and form new bonds.
Promising candidate for research
Due to its unique structure and potential applications, it is an ideal subject for further investigation in pharmaceuticals and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 5507-27-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5507-27:
(6*5)+(5*5)+(4*0)+(3*7)+(2*2)+(1*7)=87
87 % 10 = 7
So 5507-27-7 is a valid CAS Registry Number.
5507-27-7Relevant academic research and scientific papers
Nucleophilic reactivity of dehydrodiferulic acid bislactone
Boshoff, Philip R.,Perold, Guido W.
, p. 735 - 745 (2007/10/02)
Despite reports to the contrary, dehydrodiferulic acid bislactone can readily undergo nucleophilic attack.Silylation affords the disilyl ether-disilyl ester of the corresponding bismethylenesuccinic acid.Slow dissolution of the bislactone in sodium hydrogen carbonate solution affords this parent diacid, characterised as its mono- and dimethyl esters, and by its methylation to bisveratrylidenesuccinic acid, whose anhydride on aerial oxidation yields 6,7-dimethoxy-1-(3',4'-dimethoxyphenyl)naphthalene-2,3-dicarboxylic anhydride.
