59724-85-5 Usage
Uses
Used in Pharmaceutical Industry:
(CARBOXYMETHYL)[(4-METHYLPHENYL)SULFONYL]AMINOACETIC ACID is used as a building block for the synthesis of novel drugs due to its unique chemical structure and functional groups.
Used in Non-Steroidal Anti-Inflammatory Agents:
In the pharmaceutical industry, (CARBOXYMETHYL)[(4-METHYLPHENYL)SULFONYL]AMINOACETIC ACID is used as a key component in the development of non-steroidal anti-inflammatory agents, leveraging its chemical properties to create effective medications for pain and inflammation.
Used in Antibiotic Development:
(CARBOXYMETHYL)[(4-METHYLPHENYL)SULFONYL]AMINOACETIC ACID is also used as a potential candidate for the development of new antibiotics, as its sulfonamide functional group suggests it may possess antimicrobial properties, which could be beneficial in creating novel treatments for bacterial infections.
Further studies on the biological activities and potential applications of (CARBOXYMETHYL)[(4-METHYLPHENYL)SULFONYL]AMINOACETIC ACID are necessary to fully comprehend its properties and possible uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 59724-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59724-85:
(7*5)+(6*9)+(5*7)+(4*2)+(3*4)+(2*8)+(1*5)=165
165 % 10 = 5
So 59724-85-5 is a valid CAS Registry Number.
59724-85-5Relevant academic research and scientific papers
Strecker-type reaction catalyzed by carboxylic acids in aqueous media
Xie, Zhengfeng,Li, Guilong,Zhao, Gang,Wang, Jide
experimental part, p. 2035 - 2039 (2009/12/27)
Carboxylic acid catalyzed Strecker-type reactions were successfully carried out by simply mixing aldehydes, amines, tributyltin cyanide and carboxylic acid in aqueous media at room temperature, to afford α-aminonitriles in high yields. Georg Thieme Verlag
Process for preparing substituted polyazamacrocycles
-
, (2008/06/13)
A process for preparing a substituted polyazamacrocycle is provided which comprises contacting a diamine or triamine and a dicarboxylic acid or ester or anhydride thereof in the presence of a suitable base and a suitable solvent to produce the substituted
SYNTHESIS OF MACROHETEROCYCLES - ANALOGS OF DIBENZO-CROWN COMPOUNDS. 2. 18-MEMBERED DIOXADIAZA-CROWN COMPOUNDS
Formanovskii, A. A.,Mikhura, I. V.,Sokolovskii, S. A.,Murakhovskaya, A. S.,Terent'ev, P. B.,Sharbatyan, P. A.
, p. 930 - 936 (2007/10/02)
Macrocyclic diamides were synthesized by condensation of bridged 1,7-bis(2-aminophenyl)-1,7-dioxaheptanes that contain an additional donor oxygen or nitrogen atom in the bridge with glutaric, diglycolic, and N-tosyliminodiacetic acid dichlorides under hig
