15996-16-4 Usage
Description
2,5-Piperazinedione,3,6-bis(hydroxymethyl)-,trans-(8CI,9CI), also known as (3S,6R)-3,6-Bis(hydroxymethyl)piperazine-2,5-dione, is an organic compound that serves as a valuable intermediate in the synthesis of various biologically active molecules. Its unique chemical structure allows it to be a key component in the development of pharmaceuticals and other bioactive substances.
Uses
Used in Pharmaceutical Industry:
2,5-Piperazinedione,3,6-bis(hydroxymethyl)-,trans-(8CI,9CI) is used as a synthetic intermediate for the development of biologically active molecules. Its role in the pharmaceutical industry is crucial, as it contributes to the creation of new drugs and therapies that can potentially treat a wide range of medical conditions.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2,5-Piperazinedione,3,6-bis(hydroxymethyl)-,trans-(8CI,9CI) is utilized as a building block for the assembly of more complex molecules. Its versatile structure enables chemists to modify and functionalize it in various ways, leading to the formation of novel compounds with potential applications in different industries, such as agriculture, materials science, and environmental science.
Used in Research and Development:
2,5-Piperazinedione,3,6-bis(hydroxymethyl)-,trans-(8CI,9CI) is also employed in research and development laboratories, where it is used to study the properties and behavior of biologically active molecules. This knowledge can be applied to design and develop new drugs, materials, and technologies that can benefit society in various ways.
Check Digit Verification of cas no
The CAS Registry Mumber 15996-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,9 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15996-16:
(7*1)+(6*5)+(5*9)+(4*9)+(3*6)+(2*1)+(1*6)=144
144 % 10 = 4
So 15996-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O4/c9-1-3-5(11)8-4(2-10)6(12)7-3/h3-4,9-10H,1-2H2,(H,7,12)(H,8,11)
15996-16-4Relevant articles and documents
Facile Synthesis of Cyclic Dipeptides and Detection of Racemization
Ueda, Toshihisa,Saito, Morinobu,Kato, Tetsuo,Izumiya, Nobuo
, p. 568 - 572 (2007/10/02)
Several cyclic dipeptides were synthesized by refluxing methanolic solution of dipeptide methyl esters in high yield and purity.Cyclic dipeptides prepared by the Fischer method, the Nitecki method, and the present methanol-reflux method were compared with
