93434-36-7 Usage
Derivative of benzoic acid
This compound is derived from benzoic acid, which is a building block for many pharmaceuticals and a known anti-inflammatory agent.
2-Methoxyphenyl group attached to the ethyl chain
This compound contains a 2-methoxyphenyl group attached to an ethyl chain, which is responsible for its structural similarities to other bioactive compounds.
Potential therapeutic agent
2-[2-(2-METHOXYPHENYL)ETHYL]BENZOIC ACID is used in pharmaceutical and medical research as a potential therapeutic agent due to its structural similarities to other bioactive compounds.
Potential anti-inflammatory and analgesic properties
This compound has been investigated for its potential to reduce inflammation and relieve pain.
Subject of interest in drug development and medicinal chemistry research
The structure and properties of 2-[2-(2-METHOXYPHENYL)ETHYL]BENZOIC ACID make it a subject of interest in the field of drug development and medicinal chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 93434-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93434-36:
(7*9)+(6*3)+(5*4)+(4*3)+(3*4)+(2*3)+(1*6)=137
137 % 10 = 7
So 93434-36-7 is a valid CAS Registry Number.
93434-36-7Relevant articles and documents
(R, S)-2-[ [5-(9- [...] carbonyl amino) dibenzo [A, D] cyclohepta-2-yl] oxy] acetic acid synthesis process (by machine translation)
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Paragraph 0040; 0042, (2017/09/19)
The invention relates to a (R, S)-2-[ [5-(9- [...] carbonyl amino) dibenzo [A, D] cyclohepta-2-yl] oxy] acetic acid synthesis process, comprising the following steps: step one, O-carboxybenzaldehyde and Intergovernmental methoxylphenylboronic acetic acid in anhydrous sodium acetate under the catalysis of the reaction to obtain 2-(3-methoxy-vinyl) benzoic acid, Pd-C under the catalysis of the hydrogen reduction reaction-; step two, and SOCl 2 reaction to obtain 2-methoxy -10, 11-dihydro -5H-dibenzo [a, d] cycloheptene-5-one, then anhydrous AlCl 3 catalytic reflux reaction; step three, the return reaction of the intermediate product and bromine second grade acid benzyl ester for reaction; step four, the reduction reaction of the hydrogen gas, and then with Fmoc-NH 2 for reaction, to obtain. This invention, through optimization of the catalyst, is obviously improved the overall yield, effectively reducing the cost, is suitable for industrial mass synthesis application. (by machine translation)
