30508-78-2 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4-DIAMINO-6-[3-(TRIFLUOROMETHYL)PHENYL]-1,3,5-TRIAZINE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Synthesis:
This triazine derivative is also utilized in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products that can improve crop yields and protect plants from pests and diseases.
Used in Cancer Treatment Research:
2,4-DIAMINO-6-[3-(TRIFLUOROMETHYL)PHENYL]-1,3,5-TRIAZINE has been studied for its potential use in the treatment of cancer. Its biological activity and unique structure make it a promising candidate for further research and development in oncology.
Used in Drug Discovery:
As a triazine derivative with potential biological activity, 2,4-DIAMINO-6-[3-(TRIFLUOROMETHYL)PHENYL]-1,3,5-TRIAZINE is of interest to researchers in the fields of medicinal chemistry and drug discovery. Its unique properties may lead to the development of new therapeutic agents for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 30508-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,0 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30508-78:
(7*3)+(6*0)+(5*5)+(4*0)+(3*8)+(2*7)+(1*8)=92
92 % 10 = 2
So 30508-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8F3N5/c11-10(12,13)6-3-1-2-5(4-6)7-16-8(14)18-9(15)17-7/h1-4H,(H4,14,15,16,17,18)
30508-78-2Relevant academic research and scientific papers
Model Systems for Flavoenzyme Activity. Regulation of Flavin Recognition via Modulation of Receptor Hydrogen-Bond Donor-Acceptor Properties
Deans, Robert,Cooke, Graeme,Rotello, Vincent M.
, p. 836 - 839 (2007/10/03)
We have synthesized a new family of receptors for flavins based on 6-aryl-2,4-(acyldiamino)-s-triazines. In these synthetic hosts, systematic variation of the spatially remote substituents on the 6-aryl ring alters the hydrogen-bond-donating abilities of the amide functionality and the hydrogen-bond-accepting properties of the triazine N(3). This variation results in a strong modulation of the efficiency of flavin binding, with association constants for the receptor flavin complexes ranging over an 8-fold range.
