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3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-1-phenyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74979-69-4

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74979-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74979-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,7 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74979-69:
(7*7)+(6*4)+(5*9)+(4*7)+(3*9)+(2*6)+(1*9)=194
194 % 10 = 4
So 74979-69-4 is a valid CAS Registry Number.

74979-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-4-(3-nitro-phenyl)-1-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester

1.2 Other means of identification

Product number -
Other names 2,6-Dimethyl-4-(3-nitro-phenyl)-1-phenyl-1,4-dihydro-pyridin-3,5-dicarbonsaeure-diaethylester

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:74979-69-4 SDS

74979-69-4Downstream Products

74979-69-4Relevant academic research and scientific papers

Synthesis and 3D-QSAR study of 1,4-dihydropyridine derivatives as MDR cancer reverters

Radadiya, Ashish,Khedkar, Vijay,Bavishi, Abhay,Vala, Hardevsinh,Thakrar, Shailesh,Bhavsar, Dhairya,Shah, Anamik,Coutinho, Evans

, p. 375 - 387 (2014/02/14)

A series of symmetrical and unsymmetrical 1,4-dihydropyridines were synthesized by a rapid, single pot microwave irradiation (MWI) based protocol along with conventional approach and characterized by NMR, IR and mass spectroscopic techniques. The compound

Novel synthese of heterocycles with N-(1-haloalkyl)azinium halides. Part 5. Preparation of N-substituted 1,4-dihydropyridines

Vanden Eynde,Mayence,Maquestiau,Anders

, p. 3291 - 3304 (2007/10/02)

Thirty N-substituted Hantzsch 1,4-dihydropyridines were prepared under mild and neutral conditions from N-substituted enaminocarbonyl derivatives and aldehydes activated under the form of N-(1-chloroalkyl)pyridinium chlorides by means of thionyl chloride

1-ARYL- AND 1-BENZYL-3,5-DIETHOXYCARBONYL-1,4-DIHYDROPYRIDINES

Sausin, A.E.,Chekavichus, B.S.,Lusis, V.K.,Dubur, G.Ya.

, p. 377 - 385 (2007/10/02)

The possibility has been studied of using anilines in the Hantzsch synthesis.It has been shown that, with the exception of those containing strong electron-accepting substituents, they take part in this reaction with the formation of 1-aryl-1,4-dihydropyridines.The reaction largely depends on the nature of the substituents in the aniline and in the benzaldehyde and is promoted by electron-accepting substituents in the aldehyde and electron-donating substituents in the amine.The mechanism of the reaction is discussed.A number of 1-benzyl-1,4-dihydroxypyridines have been synthesized.The UV, IR, and PMR spectra and the electro-oxidation of the compounds obtained have been studied.

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