54057-49-7 Usage
Description
Benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]-, is a chemical compound with the molecular formula C13H8Cl2N2O2. It is a derivative of benzoic acid that features a 3,5-dichlorobenzoyl amino group. Benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]is known for its versatile applications across various industries due to its unique chemical structure and properties.
Uses
Used in Pharmaceutical Synthesis:
Benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]-, is utilized as an intermediate in the synthesis of various pharmaceuticals. Its specific chemical structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]-, serves as a building block for the creation of pesticides and other agricultural chemicals. Its inclusion in these products helps to enhance their effectiveness in protecting crops and managing pests.
Used in Dye Manufacturing:
Benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]is also employed in the production of dyes, where its chemical properties contribute to the colorfastness and stability of the dyes in various applications, including textiles and other industrial processes.
Used as a Preservative in Food and Cosmetics:
Due to its antimicrobial properties, benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]-, is used as a preservative in the food and cosmetics industries. It helps to prevent the growth of bacteria, mold, and yeast, thereby extending the shelf life and maintaining the quality of products.
Used in Antifungal Applications:
Research has indicated that benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]-, possesses potential antifungal properties. This makes it a candidate for use in applications where control of fungal growth is necessary, such as in medical treatments or in the preservation of materials susceptible to fungal decay.
Used in Anti-inflammatory Research:
Benzoic acid, 4-[(3,5-dichlorobenzoyl)amino]has also been studied for its potential anti-inflammatory effects. If proven effective, it could be incorporated into treatments for various inflammatory conditions, offering a new avenue for therapeutic intervention.
Check Digit Verification of cas no
The CAS Registry Mumber 54057-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,5 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54057-49:
(7*5)+(6*4)+(5*0)+(4*5)+(3*7)+(2*4)+(1*9)=117
117 % 10 = 7
So 54057-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H9Cl2NO3/c15-10-5-9(6-11(16)7-10)13(18)17-12-3-1-8(2-4-12)14(19)20/h1-7H,(H,17,18)(H,19,20)