17560-54-2 Usage
Description
2-(acetylamino)-5-(aminosulphonyl)-4-chlorobenzoic acid is a chemical compound with the molecular formula C11H11ClN2O5S. It is a derivative of salicylic acid, featuring an acetyl group, an amino group, a sulfonyl group, and a chlorine atom attached to a benzene ring. This versatile compound possesses anti-inflammatory and analgesic properties, making it a promising candidate for pharmaceutical applications. Its functional groups, including acetyl, amino, and sulfonyl, enable it to undergo various chemical reactions and modifications, further expanding its potential uses.
Uses
Used in Pharmaceutical Industry:
2-(acetylamino)-5-(aminosulfonyl)-4-chlorobenzoic acid is used as an active pharmaceutical ingredient for its anti-inflammatory and analgesic properties. It can be formulated into medications to treat conditions such as pain, inflammation, and fever, providing relief to patients suffering from various ailments.
Used in Organic Synthesis:
2-(acetylamino)-5-(aminosulphonyl)-4-chlorobenzoic acid serves as a building block in the synthesis of other organic compounds. Its functional groups allow for further chemical reactions and modifications, making it a valuable precursor in the development of new pharmaceuticals, agrochemicals, or other specialty chemicals.
Used in Drug Delivery Systems:
Innovative drug delivery systems can be developed using 2-(acetylamino)-5-(aminosulphonyl)-4-chlorobenzoic acid to enhance its bioavailability, targeting, and therapeutic efficacy. By incorporating this compound into nanoparticles, liposomes, or other carriers, its delivery to specific sites of action can be improved, potentially reducing side effects and increasing the overall effectiveness of treatments.
Used in Research and Development:
2-(acetylamino)-5-(aminosulphonyl)-4-chlorobenzoic acid is utilized in research and development for the discovery of new drug candidates and the study of its chemical properties. Its unique structure and functional groups make it an interesting subject for exploring novel reactions, mechanisms, and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 17560-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,6 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17560-54:
(7*1)+(6*7)+(5*5)+(4*6)+(3*0)+(2*5)+(1*4)=112
112 % 10 = 2
So 17560-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClN2O5S/c1-4(13)12-7-3-6(10)8(18(11,16)17)2-5(7)9(14)15/h2-3H,1H3,(H,12,13)(H,14,15)(H2,11,16,17)
