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58913-46-5

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58913-46-5 Usage

General Description

6,6-dimethyl-4-(phenylamino)-5,6-dihydropyridine-2(1H)-thione is a chemical compound with a molecular formula C13H15NOS. It is a dihydropyridine derivative and is commonly used in the synthesis of pharmaceutical compounds. The compound has been studied for its potential biological and pharmacological activities, including antihypertensive and calcium channel blocker properties. It belongs to the class of organic compounds known as thiohydantoins and is a yellowish powder with a characteristic odor. This chemical has a wide range of potential applications in the fields of medicine and pharmaceuticals due to its unique structure and properties.

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.

58913-46-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-anilino-2,2-dimethyl-1,3-dihydropyridine-6-thione

1.2 Other means of identification

Product number -
Other names 4-anilino-6,6-dimethyl-5,6-dihydro-1H-pyridine-2-thione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58913-46-5 SDS

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

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