180537-84-2 Usage
Chemical family
2,6-diamino-4-isopropyl-3,5-dicyano-4H-thiopyran belongs to the thiopyran family of compounds.
Compound structure
It is a heterocyclic compound with a 4H-thiopyran ring structure.
Functional groups
The compound contains two amino groups, an isopropyl group, and two cyano groups.
Usage
It is mainly used in the fields of organic chemistry and pharmaceuticals for the synthesis of various compounds.
Potential applications
Due to its unique structure, 2,6-diamino-4-isopropyl-3,5-dicyano-4H-thiopyran has potential applications in the development of new drugs and organic materials.
Medicinal properties
The compound has been studied for its anti-cancer and anti-inflammatory properties, making it an interesting target for further research in medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 180537-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,5,3 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 180537-84:
(8*1)+(7*8)+(6*0)+(5*5)+(4*3)+(3*7)+(2*8)+(1*4)=142
142 % 10 = 2
So 180537-84-2 is a valid CAS Registry Number.
180537-84-2Relevant academic research and scientific papers
Synthesis of 4-alkyl-6-amino-3,5-dicyano-2(1H)-pyridinethiones
Dyachenko,Krivokolysko,Nesterov,Litvinov
, p. 1430 - 1437 (2007/10/03)
Condensation of aliphatic aldehydes with cyanothioacetamide has given 4-alkyl-6-amino-3,5-dicyano-2(1H)-pyridinethiones, which have also been synthesized by recyclization of 4-alkyl-2,6-diamino-4H-thiopyrans. Substituted 2-alkylthiopyridines and thieno[2,3-b]pyridines have been prepared from the pyridinethiones. 2,6-Diamino-4-isopropyl-3,5-dicyano-4H-thiopyran and 6-amino-4-isobutyl-2-methylthio-3,5-dicyanopyridine have been studied by x-ray crystallography. 1998 Plenum Publishing Corporation.
The use of aliphatic aldehydes for the synthesis of 4-alkyl-6-amino-3,5-dicyanopyridine-2(1h)-thiones
Frolova,Zav'yalova,Litvinov
, p. 893 - 897 (2007/10/03)
The condensation of aliphatic aldehydes with malononitrile and cyanothioacetamide gives 4-alkyl-2,6-diamino-3,5-dicyano-4H-thiopyrans which recyclize into 4-alkyl-6-amino-3,5-dicyanopyridine-2(1H)-thiones. The latter are easily S-alkylated with α-haloacetonitriles and α-haloacetophenones.
