181517-09-9 Usage
Uses
Used in Pharmaceutical Industry:
1,1'-CarbonyldiiMidazole-13C is used as a catalyst for the synthesis of peptides, facilitating the formation of peptide bonds in the pharmaceutical industry. This is crucial for the development of new drugs and therapeutic agents, as peptides play a significant role in various biological processes and can be used to target specific diseases and conditions.
Used in Research and Development:
In the field of research and development, 1,1'-CarbonyldiiMidazole-13C is utilized as a labeled compound to study the mechanisms of peptide bond formation and to investigate the properties of various peptides. This can help researchers understand the structure-function relationships of peptides and develop more effective drugs and therapies.
Used in Chemical Synthesis:
1,1'-CarbonyldiiMidazole-13C is also used as a catalyst in the chemical synthesis of various compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its ability to facilitate peptide bond formation makes it a valuable tool in the synthesis of complex molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 181517-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,5,1 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 181517-09:
(8*1)+(7*8)+(6*1)+(5*5)+(4*1)+(3*7)+(2*0)+(1*9)=129
129 % 10 = 9
So 181517-09-9 is a valid CAS Registry Number.
181517-09-9Relevant articles and documents
Synthesis of isotopically labelled DNA degradation products for use in mass spectrometric studies of cellular DNA damage
Nelson, Victor C.
, p. 713 - 723 (1996)
Thirteen substituted purines and pyrimidines bearing from three to five carbon, nitrogen and/or deuterium isotopic labels have been synthesized in yields ranging from 1 to 70%. Most of the products originate from the same small number of commercially available labelled starting materials, and in several cases one intermediate leads to two products, thus minimizing the expense and time required. The parent compounds are found in tissue as the result of DNA damage often linked with carcinogenesis and mutagenesis. The synthesized compounds serve as internal standards for the study of DNA damage using mass spectrometry.
