29098-18-8 Usage
Description
(Benzoyloxy)methyl 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate is a complex organic molecule characterized by the presence of a benzoyloxy methyl group and a 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate group. (benzoyloxy)methyl 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate's structure, featuring benzoyloxy and amino groups, indicates potential applications in the pharmaceutical and organic synthesis industries. The dichloro and methyl groups further contribute to the compound's unique properties, which may have implications in organic chemistry and materials science. Further investigation and analysis are necessary to determine the specific properties and potential uses of this compound.
Uses
Used in Pharmaceutical Industry:
(Benzoyloxy)methyl 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate is used as an active pharmaceutical ingredient for its potential therapeutic effects. (benzoyloxy)methyl 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate's structure, with its benzoyloxy and amino groups, suggests it may interact with biological targets, making it a candidate for the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (benzoyloxy)methyl 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate can be used as a key intermediate or building block for the synthesis of more complex molecules. Its unique structure, including the dichloro and methyl groups, may facilitate the creation of novel compounds with specific properties and applications.
Used in Materials Science:
(benzoyloxy)methyl 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate's structural features, such as the dichloro and methyl groups, may also make it suitable for applications in materials science. (Benzoyloxy)methyl 2-[(2,6-dichloro-3-methylphenyl)amino]benzoate could potentially be utilized in the development of new materials with specific properties, such as improved stability or reactivity, depending on the requirements of various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 29098-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,9 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29098-18:
(7*2)+(6*9)+(5*0)+(4*9)+(3*8)+(2*1)+(1*8)=138
138 % 10 = 8
So 29098-18-8 is a valid CAS Registry Number.
29098-18-8Relevant articles and documents
New esters of N arylanthranilic acids
Salimbeni,Manghisi,Magistretti
, p. 276 - 286 (2007/10/06)
A series of acyloxy and alkyloxymethyl esters of meclofenamic, flufenamic and mefenamic acids has been synthesized and its antiinflammatory, analgesic and antipyretic activities have been compared with those of the corresponding acids and the methyl, β,γ isopropylidenedioxypropyl, and N,N diethylaminoethyl esters. The acyloxy and alkyloxymethyl esters are the most interesting compounds, because they possess pharmacological activity of the same order as that of the corresponding acids and a lower toxicity. The ethoxymethyl ester of N (2,6 dichloro m tolyl)anthranilic acid is presently under clinical investigation.
