127118-64-3 Usage
Thiopyran derivative
A compound derived from a thiopyran ring, which is a five-membered heterocyclic ring containing one sulfur atom and one oxygen atom.
Two amino groups
The presence of two nitrogen atoms bonded to hydrogen atoms, which can participate in hydrogen bonding and form ionic or covalent bonds with other molecules.
Two nitrile groups
The presence of two carbon atoms triple-bonded to nitrogen atoms, which can act as electron-withdrawing groups and influence the reactivity of the compound.
Potential pharmaceutical applications
The compound's structural features and biological activities make it a promising candidate for the development of novel drugs or as a building block in organic synthesis.
Further research needed
Additional studies are required to explore the compound's potential uses in the field of medicinal chemistry, including its pharmacokinetics, pharmacodynamics, and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 127118-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,1 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127118-64:
(8*1)+(7*2)+(6*7)+(5*1)+(4*1)+(3*8)+(2*6)+(1*4)=113
113 % 10 = 3
So 127118-64-3 is a valid CAS Registry Number.
127118-64-3Relevant articles and documents
Multicomponent Synthesis of 4-Alkyl(Aryl, Hetaryl)-2-alkoxycarbonyl(aroyl, carbamoyl)- 3,6-diamino-5-cyanothieno[2,3-b]pyridines
Dyachenko,Dyachenko,Dorovatovskii,Khrustalev,Nenajdenko
, p. 1435 - 1445 (2019/01/04)
The condensation of malononitrile with hydrogen sulfide and aldehydes in the presence of triethylamine in ethanol at room temperature afforded 4-alkyl(aryl, hetaryl)-2,6-diamino-3,5-dicyano-4H-thiopyrans. Treatment of the latter in situ with alkali in DMF, followed by addition of an alkylating agent, led to the formation of 4-alkyl(aryl, hetaryl)-2-alkoxycarbonyl(aroyl, carbamoyl)-3,6-diamino-5-cyanothieno[2,3-b]- pyridines.
