62770-06-3 Usage
Uses
Used in Pharmaceutical Industry:
(2-MORPHOLIN-4-YL-2-OXO-ETHYLSULFANYL)-ACETIC ACID serves as an intermediate in the synthesis of various pharmaceuticals, leveraging its unique structural features to contribute to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (2-MORPHOLIN-4-YL-2-OXO-ETHYLSULFANYL)-ACETIC ACID is utilized as an intermediate in the production of agrochemicals, potentially enhancing the effectiveness of pesticides, herbicides, and other agricultural chemicals.
Used in Organic Synthesis:
(2-MORPHOLIN-4-YL-2-OXO-ETHYLSULFANYL)-ACETIC ACID is employed as a sulfur-containing building block in organic synthesis, providing a foundation for the creation of complex organic molecules and compounds with specific properties and applications.
Used in the Formation of Amides and Esters:
The carboxylic acid group present in (2-MORPHOLIN-4-YL-2-OXO-ETHYLSULFANYL)-ACETIC ACID allows it to be used in the formation of amides and esters, which are essential in various chemical reactions and have applications in industries such as plastics, textiles, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 62770-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,7 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62770-06:
(7*6)+(6*2)+(5*7)+(4*7)+(3*0)+(2*0)+(1*6)=123
123 % 10 = 3
So 62770-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO4S/c10-7(5-14-6-8(11)12)9-1-3-13-4-2-9/h1-6H2,(H,11,12)/p-1
62770-06-3Relevant academic research and scientific papers
New broad spectrum alkylthio cephalosporins
Nannini,Molgora,Biasoli
, p. 343 - 352 (2007/10/05)
A series of 7 substituted alkyl thio acylaminocephalosporins were prepared and tested for in vitro antibacterial activity. The authors tried in their research to find any relationship between antibacterial activity and pharmacokinetic properties on the one hand, and chemical structure on the other. The most interesting products were also studied for their in vivo antibacterial activity in experimental acute systemic infections in the mouse.
