33924-53-7 Usage
Uses
Used in Pharmaceutical Industry:
p-[2-[(5-Chloro-2-methoxybenzoyl)amino]ethyl]benzenesulfonic Acid is used as a membrane-impermeant Glibenclamide analogue for its potential application in the development of drugs targeting specific receptors or ion channels. Its unique structure allows it to interact with biological targets in a controlled manner, making it a valuable compound in the field of medicinal chemistry.
Used in Chemical Research:
In the realm of chemical research, p-[2-[(5-Chloro-2-methoxybenzoyl)amino]ethyl]benzenesulfonic Acid serves as a valuable compound for studying various chemical reactions and mechanisms. Its distinct functional groups and structural features make it an interesting subject for exploring new synthetic pathways and understanding the reactivity of different molecular moieties.
Used in Material Science:
The unique properties of p-[2-[(5-Chloro-2-methoxybenzoyl)amino]ethyl]benzenesulfonic Acid also make it a candidate for use in material science, where it could be employed in the development of novel materials with specific properties. Its chemical structure may allow for the creation of materials with tailored characteristics, such as improved stability, reactivity, or selectivity in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 33924-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,2 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33924-53:
(7*3)+(6*3)+(5*9)+(4*2)+(3*4)+(2*5)+(1*3)=117
117 % 10 = 7
So 33924-53-7 is a valid CAS Registry Number.
33924-53-7Relevant academic research and scientific papers
CRYOPYRIN INHIBITORS FOR PREVENTING AND TREATING INFLAMMATION
-
Page/Page column title; sheet 3, (2014/12/12)
Inhibitors that are anti-inflammatory agents are provided, as are methods of using the analogs to inhibit inflammation and prevent or treat diseases and conditions associated with inflammation, such as heart failure and autoimmune diseases.
Process for preparing p-(5-chloro-2-methoxy-benzamidoethyl)-benzene sulfonamide
-
, (2008/06/13)
A process for preparing p-[5-chloro-2-methoxy-benzamidoethyl]-benzene sulfonamide consisting of treating 5-chlorosalicylic acid or its ester by methylating and aminolysis to form N-phenethyl-5-chloro-2-methoxybenzamide followed by chlorosulfonation and aminolysis.
