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38880-90-9

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38880-90-9 Usage

General Description

4'-Amino-2'-hydroxybenzanilide, also known as N-(4-aminophenyl)-salicylamide, is a chemical compound that belongs to the class of anilides. It is a white to off-white crystalline powder that is sparingly soluble in water. 4'-Amino-2'-hydroxybenzanilide is commonly used in the manufacturing of pharmaceuticals and also has applications in the field of organic synthesis. It is known for its antipyretic and analgesic properties, and has been the subject of research for its potential therapeutic use in treating inflammatory and pain-related conditions. Additionally, 4'-Amino-2'-hydroxybenzanilide has shown to exhibit antioxidant properties and has been studied for its potential use in developing antioxidant-based therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 38880-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,8 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38880-90:
(7*3)+(6*8)+(5*8)+(4*8)+(3*0)+(2*9)+(1*0)=159
159 % 10 = 9
So 38880-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O2/c14-10-6-7-11(12(16)8-10)15-13(17)9-4-2-1-3-5-9/h1-8,16H,14H2,(H,15,17)

38880-90-9Relevant articles and documents

Synthesis and biological evaluation of new N-(2-hydroxy-4(or 5)-nitro/aminophenyl)benzamides and phenylacetamides as antimicrobial agents

Ertan, Tugba,Yildiz, Ilkay,Ozkan, Semiha,Temiz-Arpaci, Ozlem,Kaynak, Fatma,Yalcin, Ismail,Aki-Sener, Esin,Abbasoglu, Ufuk

, p. 2032 - 2044 (2007/10/03)

A new series of N-(2-hydroxy-4(or 5)-nitro/aminophenyl)benzamide and phenylacetamide derivatives (1a-1n, 2a-2n) were synthesized and evaluated for antibacterial and antifungal activities against Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae, Pseudomonas aeruginosa, Escherichia coli, Candida albicans, and their drug-resistant isolate. Microbiological results indicated that the compounds possessed a broad spectrum of activity against the tested microorganisms at MIC values between 500 and 1.95 μg/ml. Benzamide derivative 1d exhibited the greatest activity with MIC values of 1.95, 3.9, and 7.8 μg/ml against drug-resistant B. subtilis, B. subtilis, and S. aureus, respectively.

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