58913-46-5 Usage
Description
6,6-dimethyl-4-(phenylamino)-5,6-dihydropyridine-2(1H)-thione is a dihydropyridine derivative with a molecular formula C13H15NOS. It is a yellowish powder with a characteristic odor and belongs to the class of organic compounds known as thiohydantoins. This chemical compound is commonly used in the synthesis of pharmaceutical compounds and has been studied for its potential biological and pharmacological activities, including antihypertensive and calcium channel blocker properties.
Uses
Used in Pharmaceutical Industry:
6,6-dimethyl-4-(phenylamino)-5,6-dihydropyridine-2(1H)-thione is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential biological and pharmacological activities.
Used in Cardiovascular Applications:
In the pharmaceutical industry, 6,6-dimethyl-4-(phenylamino)-5,6-dihydropyridine-2(1H)-thione is used as an active pharmaceutical ingredient for the development of antihypertensive and calcium channel blocker drugs. Its unique structure and properties contribute to its ability to regulate blood pressure and improve cardiovascular health.
Used in Drug Discovery and Research:
6,6-dimethyl-4-(phenylamino)-5,6-dihydropyridine-2(1H)-thione is utilized as a research compound in drug discovery and development. Its potential biological activities make it a valuable tool for studying the mechanisms of action and therapeutic effects of new drug candidates in the field of medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 58913-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,1 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58913-46:
(7*5)+(6*8)+(5*9)+(4*1)+(3*3)+(2*4)+(1*6)=155
155 % 10 = 5
So 58913-46-5 is a valid CAS Registry Number.
58913-46-5Relevant articles and documents
Synthesis of new tetrahydropyridinylidene ammonium salts and their antiprotozoal potency
Seebacher, Werner,Faist, Johanna,Weis, Robert,Saf, Robert,Belaj, Ferdinand,Kaiser, Marcel,Brun, Reto
, p. 1299 - 1308 (2015)
Several new tetrahydropyridinylidene ammonium salts were prepared by selective reduction. They were characterized using UV-Vis spectroscopy, FT-IR spectroscopy, and HRMS. Their structure was established by NMR spectroscopy and a single X-ray structure ana
4-Hydroxy-6,6-dimethyl-5,6-dihydro-2(1H)-pyridinethione and -one and the Corresponding Tautomers
Zigeuner, Gustav,Schweiger, Klaus,Fuchsgruber, Alfred
, p. 187 - 198 (2007/10/02)
The tautomers, 4-hydroxy-5,6-dihydro-6,6-dimethyl-2(1H)-pyridinethione (1) and 6,6-dimethyl-2-thioxo-4-piperidone (2) resp., and 4-hydroxy-5,6-dihydro-6,6-dimethyl-2(1H)-pyridone (9) and 6,6-dimethyl-2,4-piperidinedione (10) resp. were synthesized by hydrolysis of 4-amino-5,6-dihydro-6,6-dimethyl-2(1H)-pyridinethiones (4,5) and -ones (11,12). 1,2 and 9,10 undergo an aminolysis in amines to the corresponding 4-aminodihydro-2(1H)-pyridinethiones 4,5 and -ones 11, 12 resp. - Keywords: 6,6-Dimethyl-2,4-piperidindione; 6,6-Dimethyl-2-thioxo-4-piperidone; 4-Hydroxy-6,6-dimethyl-5,6-dihydro-2(1H)-pyridone, and -pyridinethione; Keto-enol-tautomeris m
