40860-26-2 Usage
General Description
2-[(Aminocarbonyl)amino]pentanedioic acid is a chemical compound with the molecular formula C8H14N2O6. It is commonly referred to as aminocaproic acid, and is an analogue of the amino acid lysine. It is a synthetic derivative of the amino acid lysine, and is used as an antifibrinolytic agent to prevent excessive bleeding during surgery or trauma. Aminocaproic acid works by inhibiting the activation of plasminogen, a protein involved in the breakdown of blood clots. It is also used to treat certain types of clotting disorders and can be administered orally or intravenously. Additionally, it has been investigated for potential use in the treatment of neurodegenerative diseases and cystic fibrosis.
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 articles and documents
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.
