40856-73-3 Usage
Uses
Used in Organic Synthesis:
(S)-5-Methylhydantoin is used as a synthetic building block for the creation of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable asset in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-5-Methylhydantoin is used as an intermediate in the synthesis of various drugs. Its ability to undergo multiple chemical transformations makes it a key component in the development of new medications with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
(S)-5-Methylhydantoin is also employed in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its versatility in organic synthesis enables the development of novel compounds with enhanced pest control properties and reduced environmental impact.
Used in Research and Development:
In the field of research and development, (S)-5-Methylhydantoin serves as a valuable compound for exploring new chemical reactions and understanding the underlying mechanisms. Its unique properties make it an ideal candidate for studying various aspects of organic chemistry, including reaction kinetics, stereochemistry, and mechanistic insights.
Check Digit Verification of cas no
The CAS Registry Mumber 40856-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,5 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40856-73:
(7*4)+(6*0)+(5*8)+(4*5)+(3*6)+(2*7)+(1*3)=123
123 % 10 = 3
So 40856-73-3 is a valid CAS Registry Number.
40856-73-3Relevant academic research and scientific papers
Assembly/disassembly of drug conjugates using imide ligation
Mhidia, Reda,Beziere, Nicolas,Blanpain, Annick,Pommery, Nicole,Melnyk, Oleg
supporting information; experimental part, p. 3982 - 3985 (2010/11/02)
A strategy is described that allows the easy assembly and controlled disassembly of drug conjugates. Imide ligation, that is, the reaction of a peptide thioacid with an azidoformate, is used for conjugate assembly. The imide bond participates also with an endopeptidase-triggered cyclization-based disassembly mechanism.
