31408-17-0 Usage
Uses
Used in Pharmaceutical Industry:
5-P-TOLYLPYRIMIDIN-2-YLAMINE is used as a building block for the synthesis of various biologically active molecules, including pharmaceutical drugs. Its unique structure allows it to be a key component in the development of new therapeutic agents.
Used in Antineoplastic Applications:
In the field of oncology, 5-P-TOLYLPYRIMIDIN-2-YLAMINE is studied for its potential use as an antineoplastic agent. This means it may have the ability to inhibit the growth of cancer cells, offering a new avenue for cancer treatment.
Used in Antiviral Applications:
5-P-TOLYLPYRIMIDIN-2-YLAMINE has also been investigated for its potential use as an antiviral agent, particularly against the hepatitis C virus. Its antiviral properties could contribute to the development of new treatments for viral infections.
Overall, 5-P-TOLYLPYRIMIDIN-2-YLAMINE's diverse applications in medicine, pharmaceuticals, and research highlight its importance as a versatile chemical compound with significant potential in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 31408-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,0 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31408-17:
(7*3)+(6*1)+(5*4)+(4*0)+(3*8)+(2*1)+(1*7)=80
80 % 10 = 0
So 31408-17-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3/c1-8-2-4-9(5-3-8)10-6-13-11(12)14-7-10/h2-7H,1H3,(H2,12,13,14)
31408-17-0Relevant articles and documents
Palladium-catalyzed Suzuki cross-coupling of N′-tosyl arylhydrazines
Liu, Jin-Biao,Yan, Hui,Chen, Hui-Xuan,Luo, Yu,Weng, Jiang,Lu, Gui
supporting information, p. 5268 - 5270 (2013/07/04)
The first palladium-catalyzed Suzuki cross-coupling of N′-tosyl arylhydrazines with various organoboron reagents has been developed for the preparation of biaryl compounds in high yields. N′-Tosyl arylhydrazine as a readily available and stable electrophile also demonstrated its generality in a number of coupling reactions. The Royal Society of Chemistry 2013.