170872-51-2 Usage
Derivative of 1,2,4-triazine
The compound is derived from the parent compound 1,2,4-triazine, which is a six-membered heterocyclic ring containing three nitrogen atoms.
2-(2,3-dihydroxypropyl)-6-ethyl substituent
The compound has a specific functional group attached to the triazine ring, which includes a 2,3-dihydroxypropyl group and an ethyl group at the 6th position.
Presence of hydroxyl and ethyl groups
The compound contains hydroxyl (-OH) and ethyl (-CH2CH3) functional groups, which are common in many natural and synthetic bioactive compounds.
Biological relevance
Due to the presence of hydroxyl and ethyl groups, the compound may have potential biological relevance and could be involved in various biological processes.
Potential applications
The compound's chemical structure suggests possible applications in pharmaceuticals, agrochemicals, or materials science.
Lack of well-documented uses and properties
The specific uses and properties of 1,2,4-Triazine-3,5(2H,4H)-dione, 2-(2,3-dihydroxypropyl)-6-ethyl- (9CI) are not well-documented, indicating that further research and evaluation are needed to better understand its potential.
Need for further research
Further investigation into the compound's properties, potential applications, and biological activities may lead to a better understanding of its uses and relevance in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 170872-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,8,7 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 170872-51:
(8*1)+(7*7)+(6*0)+(5*8)+(4*7)+(3*2)+(2*5)+(1*1)=142
142 % 10 = 2
So 170872-51-2 is a valid CAS Registry Number.
170872-51-2Relevant academic research and scientific papers
Tzeng,Hwang,Chen,Wei
, p. 1425 - 1435 (1995)
Acyclic nucleoside analogues of antiviral DHPA and HPMPA have been prepared. Coupling of silylated 6-azauracils with benzyl glycidyl ether and stannic chloride followed by the deprotection with boron trichloride gave 1- (2,3-dihydroxypropyl)-6-azauracils (3) in good overall yields. Reaction of silylated 6-azauracil and epichlorohydrin with or without catalytic stannic chloride afforded 1-(2-chloro-3-hydroxypmpyl)-6-azauracil (4a) and 1-(3- chloro-2-hydroxypropyl)-6-azauracil (6a) respectively. Coupling of silylated 6-azaisocytosine under the same reaction conditions provided 1-(2,3- dihydroxypropyl)-6-azaisocytosine (9) and 1-(2-chloro-3-hydroxypropyl)-6- azaisocytosine (10) respectively. None of the compounds exhibited significant antiviral activity against herpes simplex viruses.
