14511-59-2 Usage
Description
Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate is a complex organic compound with a unique chemical structure. It is characterized by its off-white solid appearance and is known to be an impurity in the synthesis of Glyburide (G598350). The compound's specific properties and potential applications are not explicitly detailed in the provided materials, but its chemical structure suggests it may have potential uses in various industries.
Uses
Used in Pharmaceutical Industry:
Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate is used as an impurity in the synthesis of Glyburide (G598350) for the development of pharmaceutical products. Its presence in the synthesis process may affect the purity and efficacy of the final product, making it an important consideration in the manufacturing process.
Used in Chemical Research:
As a complex organic compound, Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate may also be used in chemical research for studying its properties, potential reactions, and possible applications in various fields. Researchers may explore its chemical behavior, stability, and interactions with other compounds to better understand its potential uses and limitations.
Used in Quality Control and Analysis:
The identification of Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate as an impurity in the synthesis of Glyburide (G598350) highlights its importance in quality control and analysis within the pharmaceutical industry. It may be used as a reference compound for testing and validating analytical methods, ensuring the purity and safety of the final product.
Please note that the specific applications and uses of Ethyl 4-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzene Sulfonamide Carbamate may vary depending on further research and development in the field. The provided information is based on the limited data available and should be considered as a starting point for further investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 14511-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,1 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14511-59:
(7*1)+(6*4)+(5*5)+(4*1)+(3*1)+(2*5)+(1*9)=82
82 % 10 = 2
So 14511-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H21ClN2O6S/c1-3-28-19(24)22-29(25,26)15-7-4-13(5-8-15)10-11-21-18(23)16-12-14(20)6-9-17(16)27-2/h4-9,12H,3,10-11H2,1-2H3,(H,21,23)(H,22,24)
14511-59-2Relevant articles and documents
Synthesis technology of glibenclamide
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Paragraph 0043; 0045, (2017/08/25)
The invention provides a novel synthesis technology of a glibenclamide bulk pharmaceuticals. The glibenclamide product is finally prepared by taking sulfamide as a starting raw material through the four steps of a secondary condensation reaction, a compounding reaction, a dealcoholization reaction and refining. The technology has the advantages of being high in yield, low in purity, easy and convenient to operate, suitable for industrialized production and the like.
SYNTHESIS OF 4-trans-BENZENESULFONYL>UREIDO>CYCLOHEXANOL HEMISUCCINATE ESTER
Stephon, Robert L.,Niedbala, R. Sam,Schray, Keith J.,Heindel, Ned D.
, p. 339 - 342 (2007/10/03)
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