135086-65-6 Usage
Chemical class
Heterocyclic compound
Structure
Contains a thiadiazole ring
Biological activities
Studied for various biological activities
Potential applications
a. Building block for the synthesis of novel pharmaceuticals
b. Building block for the synthesis of novel agrochemicals
c. Development of new materials
d. Tool for chemical and biochemical research
Importance
Potentially valuable compound for further investigation and development in the field of medicinal chemistry and drug discovery
Check Digit Verification of cas no
The CAS Registry Mumber 135086-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,8 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135086-65:
(8*1)+(7*3)+(6*5)+(5*0)+(4*8)+(3*6)+(2*6)+(1*5)=126
126 % 10 = 6
So 135086-65-6 is a valid CAS Registry Number.
135086-65-6Relevant academic research and scientific papers
SYNTHESIS OF NEW DERIVATIVES OF FURAZAN- AND 1,2,5-THIADIAZOLECARBOXYLIC ACIDS
Ivanov, E. I.,Yavolovskii, A. A.,Kuklenko, E. A.,Ivanova, R. Yu.
, p. 342 - 345 (2007/10/02)
A convenient method is proposed for the synthesis of the new heterocyclic system 3-ethylenediamino-1,2,5-oxadiazole-4-carboxamide and its thio analog by intramolecular alkylation of 3-(β-chloroethylamino)-1,2,5-thia(oxa)diazole-4-carboxamides.
REACTIONS OF 3-(β-HYDROXYETHYL)-8-THIAXANTHINE
Ivanov, E. I.,Yavolovskii, A. A.,Kuklenko, E. A.,Timofeev, O. S.
, p. 225 - 227 (2007/10/02)
Depending on the base used, reaction of 3-(β-hydroxyethyl)-8-thiaxanthine with p-toluenesulfonylchloride either stops at the stage of formation of the tosylate or gives 1,2,5-thiadiazolooxazolidinopyrimidin-9(4H)-one.Upon treatment with ammonia or methylamine, both of these compounds react to give 3-(β-hydroxyethyl)-8-thiaguanines.
