40288-19-5 Usage
Class
Organic compounds
Subclass
Thiadiazoles
Structure
Five-membered ring with three carbon atoms, one sulfur atom, and one nitrogen atom
Additional atoms
Chlorine atom and a 2-methoxyphenyl group attached to the thiadiazole ring
Applications
Research and development of pharmaceuticals and agrochemicals
Potential uses
Synthesis of new drugs, crop protection products, materials science, and other chemical industries
Biological activities
Not specified, but implied due to its use in pharmaceutical and agrochemical research and development
Check Digit Verification of cas no
The CAS Registry Mumber 40288-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,8 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40288-19:
(7*4)+(6*0)+(5*2)+(4*8)+(3*8)+(2*1)+(1*9)=105
105 % 10 = 5
So 40288-19-5 is a valid CAS Registry Number.
40288-19-5Relevant academic research and scientific papers
Antihypertensive Thiadiazoles. 1. Synthesis of Some 2-Aryl-5-hydrazino-1,3,4-thiadiazoles with Vasodilator Activity
Turner, Stephen,Myers, Malcolm,Gadie, Brian,Nelson, Anthony J.,Pape, Robin,et al.
, p. 902 - 906 (2007/10/02)
Some 2-Aryl-5-hydrazino-1,3,4-thiadiazoles have been synthesized and screened for antihypertensive activity.In general, compounds with a 2-substituted phenyl ring had higher activity than their 3- or 4-substituted counterparts or those containing heteroar
