41733-55-5 Usage
Description
Sodium 5-(aminosulphonyl)-4-chloro-2-(furan-2-ylmethyl)anthranilate is a complex chemical compound that integrates elements such as sodium, chlorine, nitrogen, sulfur, and carbon. It is recognized for its intricate structure and potential applications across various industries.
Uses
Used in Pharmaceutical Industry:
Sodium 5-(aminosulphonyl)-4-chloro-2-(furan-2-ylmethyl)anthranilate serves as a crucial intermediate in the synthesis of organic compounds and pharmaceuticals. Its unique structural composition allows it to be a key component in the development of new drugs and medicines.
Used in Agrochemical Industry:
Due to its distinctive properties, sodium 5-(aminosulphonyl)-4-chloro-2-(furan-2-ylmethyl)anthranilate may be utilized in the agrochemical sector. Its application could be for the development of new pesticides, herbicides, or other agricultural chemicals that require its specific chemical traits.
Used in Dye Industry:
sodium 5-(aminosulphonyl)-4-chloro-2-(furan-2-ylmethyl)anthranilate's unique structure and properties also make it a potential candidate for use in the dye industry. It could be employed in the creation of novel dyes with specific color characteristics or stability profiles.
Safety Note:
It is imperative to handle sodium 5-(aminosulphonyl)-4-chloro-2-(furan-2-ylmethyl)anthranilate with care and adhere to safety guidelines to mitigate any potential hazards associated with its use. Proper safety measures should be implemented to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 41733-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,3 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41733-55:
(7*4)+(6*1)+(5*7)+(4*3)+(3*3)+(2*5)+(1*5)=105
105 % 10 = 5
So 41733-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H11ClN2O5S.Na/c13-9-5-10(15-6-7-2-1-3-20-7)8(12(16)17)4-11(9)21(14,18)19;/h1-5,15H,6H2,(H,16,17)(H2,14,18,19);/q;+1/p-1
41733-55-5Relevant articles and documents
Preparation method of furosemide
-
Paragraph 0056, (2017/01/02)
The invention provides a preparation method of furosemide and relates to the technical field of pharmaceutical synthesis. The preparation method comprises the following steps: (1) 2,4-dichloro-5-sulfamoylbenzoic acid and alkali are subjected to a reaction in presence of an organic solvent, a reaction liquid is obtained and subjected to aftertreatment, and sodium 2,4-dichloro-5-sulfamoylbenzoic acid is obtained; (2) sodium 2,4-dichloro-5-sulfamoylbenzoic acid and furfurylamine are subjected to a reaction in presence of an organic solvent, furfurylamine and the solvent are recovered through reduced pressure distillation after the reaction, a reaction liquid is obtained and mixed with isopropyl alcohol, a mixture is stirred, crystallized and filtered, and sodium furosemide is obtained; (3) sodium furosemide is subjected to water dissolution, activated carbon decoloration and glacial acetic acid acidification, and a finished furosemide product is obtained. The preparation method has the advantages that raw materials are cheap and available, the cost is low, short time is consumed, reaction steps are short, operation is simple, product quality is good, yield is high, solvents can be recycled and reused, environmental pollution is small and the like, and the preparation method is suitable for industrial production.