40860-26-2 Usage
Uses
Used in Medical Applications:
Aminocaproic acid is used as an antifibrinolytic agent for preventing excessive bleeding during surgery or trauma. It achieves this by inhibiting the activation of plasminogen, a protein that is involved in the breakdown of blood clots, thus helping to maintain the stability of clots and prevent uncontrolled bleeding.
Used in Treatment of Clotting Disorders:
In the medical field, aminocaproic acid is utilized as a treatment for certain types of clotting disorders. It can be administered orally or intravenously, providing a therapeutic option for patients with specific clotting issues.
Used in Pharmaceutical Research:
Aminocaproic acid has been investigated for its potential use in the treatment of neurodegenerative diseases and cystic fibrosis. Its unique properties as a synthetic derivative of lysine offer opportunities for further research and development in these areas, potentially leading to new therapeutic approaches for these challenging conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 40860-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40860-26:
(7*4)+(6*0)+(5*8)+(4*6)+(3*0)+(2*2)+(1*6)=102
102 % 10 = 2
So 40860-26-2 is a valid CAS Registry Number.
40860-26-2Relevant academic research and scientific papers
A practically simple, catalyst free and scalable synthesis of: N -substituted ureas in water
Tiwari, Lata,Kumar, Varun,Kumar, Bhuvesh,Mahajan, Dinesh
, p. 21585 - 21595 (2018/06/26)
A practically simple, mild and efficient method is developed for the synthesis of N-substituted ureas by nucleophilic addition of amines to potassium isocyanate in water without organic co-solvent. Using this methodology, a variety of N-substituted ureas (mono-, di- and cyclic-) were synthesized in good to excellent yields with high chemical purity by applying simple filtration or routine extraction procedures avoiding silica gel purification. The developed methodology was also found to be suitable for gram scale synthesis of molecules having commercial application in large volumes. The identified reaction conditions were found to promote a unique substrate selectivity from a mixture of two amines.
