232941-14-9 Usage
Uses
Used in Pharmaceutical Research and Development:
Methyl 4-(acetylaMino)-3-broMo-5-chloro-2-hydroxybenzoate serves as a crucial intermediate in the synthesis of a range of pharmaceuticals. Its unique combination of functional groups allows for the development of drugs with diverse therapeutic profiles.
Used in Antibacterial Applications:
In the pharmaceutical industry, Methyl 4-(acetylaMino)-3-broMo-5-chloro-2-hydroxybenzoate is used as a building block for creating antibacterial agents. Its structure can be tailored to target specific bacterial mechanisms, contributing to the fight against antibiotic-resistant strains.
Used in Antifungal Applications:
Similarly, Methyl 4-(acetylaMino)-3-broMo-5-chloro-2-hydroxybenzoate is utilized in the development of antifungal medications, capitalizing on its ability to interfere with fungal cell processes and inhibit their growth, thereby addressing various fungal infections.
Used in Anti-inflammatory Applications:
Methyl 4-(acetylaMino)-3-broMo-5-chloro-2-hydroxybenzoate also finds use in formulating anti-inflammatory drugs, potentially modulating immune responses and reducing inflammation associated with various conditions.
Used in Organic Synthesis as a Reagent:
Beyond direct pharmaceutical applications, Methyl 4-(acetylaMino)-3-broMo-5-chloro-2-hydroxybenzoate operates as a reagent in organic synthesis. It aids in the construction of more complex molecular architectures with potential medicinal uses, expanding the scope of available treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 232941-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,2,9,4 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 232941-14:
(8*2)+(7*3)+(6*2)+(5*9)+(4*4)+(3*1)+(2*1)+(1*4)=119
119 % 10 = 9
So 232941-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9BrClNO4/c1-4(14)13-8-6(12)3-5(10(16)17-2)9(15)7(8)11/h3,15H,1-2H3,(H,13,14)
232941-14-9Relevant academic research and scientific papers
Synthetic method for prucalopride succinate intermediate 4-amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid
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, (2017/12/06)
The invention belongs to the technical field of medicines, and relates to a synthetic method for a prucalopride succinate intermediate 4-amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid. The final product 4-amino-5-chloro-2,3-dihydrobenzofuran-7-carboxylic acid is obtained by using p-aminosalicylic acid as a starting raw material, successively performing esterification, acylation, and twice halogenation to obtain 4-acetylamino-3-bromo-5-chloro-2-hydroxybenzoic acid methyl ester, then performing substitution reaction on 1,2-dibromoethane and the 4-acetylamino-3-bromo-5-chloro-2-hydroxybenzoic acid methyl ester to obtain 4-acetylamino-3-bromo-2-(2-bromoethoxy)-5-chlorobenzoic acid methyl ester, and successively performing cyclization and hydrolyzation. According to the invention, the raw materials are easy to get, the operation is simple and mild, the production period is short, the purity is high, the safety is good, the costs are low, and the synthetic method is suitable for industrialized production.
