2181-76-2 Usage
Description
2,6-Pyridinedicarboxylic acid,4-(2-(2-carboxy-2,3-dihydro-5,6-dihydroxy-1H-indol-1-yl)ethenyl)-2,3-dihydro-, (S-(R,R))is a complex organic compound characterized by the presence of a pyridine ring and a dihydroxy indolyl group. It is a stereoisomer with a specific configuration, denoted as (S-(R,R))-. This unique molecular structure endows it with potential biological activity, making it a promising candidate for pharmaceutical applications. Further research is required to explore its properties and potential uses in the development of new drugs or treatments.
Uses
Used in Pharmaceutical Industry:
2,6-Pyridinedicarboxylic acid,4-(2-(2-carboxy-2,3-dihydro-5,6-dihydroxy-1H-indol-1-yl)ethenyl)-2,3-dihydro-, (S-(R,R))is used as a pharmaceutical compound for its potential biological activity. Its unique structure and characteristics make it a subject of interest in the research and development of new drugs or treatments.
The specific applications and reasons for its use in the pharmaceutical industry are not provided in the materials. However, given its potential biological activity, it may be used for various therapeutic purposes, such as targeting specific biological pathways or receptors, modulating cellular processes, or exhibiting synergistic effects with other drugs. Further studies are needed to fully understand its properties and potential uses in the development of new drugs or treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 2181-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2181-76:
(6*2)+(5*1)+(4*8)+(3*1)+(2*7)+(1*6)=72
72 % 10 = 2
So 2181-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H16N2O8/c21-14-6-9-5-13(18(27)28)20(12(9)7-15(14)22)2-1-8-3-10(16(23)24)19-11(4-8)17(25)26/h1-3,6-7,11,13H,4-5H2,(H5,21,22,23,24,25,26,27,28)/t11-,13-/m0/s1
2181-76-2Relevant articles and documents
Chlorination of Betacyanins in Several Hypochlorous Acid Systems
Wybraniec, S?awomir,Starzak, Karolina,Pietrzkowski, Zbigniew
, p. 2865 - 2874 (2016/05/09)
This study presents a comparative evaluation of chlorination of betanin, betanidin, and neobetanin exposed to sodium hypochlorite and myeloperoxidase (MPO)/H2O2/Cl- systems. For betanin/betanidin, the chlorination takes place at the aglycone unit, but for neobetanin, no chlorinated products in the reaction mixtures can be detected. In the RP-HPLC system, monochloro-betanin/-betanidin were eluted earlier than their corresponding nonchlorinated substrates. An influence of Cl- concentration on betanin/betanidin chlorination efficiency in sodium hypochlorite and MPO systems was investigated. At pH 3-5, the yields of formed monochloro-betanin/-betanidin decrease dramatically at higher Cl- concentrations, indicating that generated Cl2 is not the chlorinating agent in the presence of sodium hypochlorite. The intriguing low activity of Cl2 in betanin/betanidin chlorination compared to HOCl and/or Cl2O can be explained by a special position of the attack by molecules of HOCl and/or Cl2O. In the MPO/H2O2/Cl- system, the highest efficiency of monochloro-betanin/-betanidin generation is observed at pH 5.
