23125-28-2

Basic information

• Product Name: 2,6-Dimethyl-4-(2-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester
• Synonyms: 1,4-Dihydro-2,6-dimethyl-4-(2-pyridyl)-3,5-pyridinedicarboxylic acid diethyl ester;2',6'-Dimethyl-1',4'-dihydro-2,4'-bipyridine-3',5'-dicarboxylic acid diethyl ester;2,6-Dimethyl-4-(2-pyridyl)-1,4-dihydro-3,5-pyridinedicarboxylic acid diethyl ester;2,6-Dimethyl-4-(2-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester;4-(2-Pyridyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester;Bay-1518;(2,4'-Bipyridine)-3',5'-dicarboxylic acid, 1',4'-dihydro-2',6'-dimethyl-, diethyl ester;(2,4'-Bipyridine)-3',5'-dicarboxylic acid, 1',4'-dihydro-2',6'-dimethyl-, diethyl ester (8ci)(9ci)
• CAS NO: 23125-28-2
• Molecular Formula: C₁₈H₂₂N₂O₄
• Molecular Weight: 330.42
• Mol File: 23125-28-2.mol
• Article Data: 28

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-Dimethyl-4-(2-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dimethyl-4-(2-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester(23125-28-2)
• EPA Substance Registry System: 2,6-Dimethyl-4-(2-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester(23125-28-2)

Safety Data

• Hazardous Substances Data: 23125-28-2(Hazardous Substances Data)

Usage

Safety Profile

A poison by intravenous route. When heated to decomposition it emits toxic vapors of NO,x

Upstream product

• 1121-60-4 pyridine-2-carbaldehyde 
• 141-97-9 ethyl acetoacetate 
• 626-34-6 ethyl 3-aminobut-2-enoate 

Downstream Products

• 78005-05-7 3',5'-Bis-ethoxycarbonyl-1,2',6'-trimethyl-1',4'-dihydro-[2,4']bipyridinyl-1-ium; iodide 
• 581-47-5 4-(2-pyridyl)pyridine 

Relevant articles and documents

Experimental and theoretical structural study of 2-pyridyl- and 4-hydroxyphenyl-1,4-dihydropyridine derivatives

A series of substituted 1,4-dihydropyridines (1,4-DHPs) has been synthesised following the well-known Hantzsch's procedure for symmetrical 1,4-DHP. The structures of these compounds have been thoroughly studied by X-ray crystallographic analysis and semie

USY-zeolite catalyzed synthesis of 1,4-dihydropyridines under microwave irradiation: structure and recycling of the catalyst

The Hantzsch three-component reaction is the best-known multicomponent reaction, affording dihydropyridines which have been employed therapeutically and also as visible‐light photoredox catalysts. In this work we report the application of an ultra-stable

Diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate derivative for inducing cell apoptosis, a method for producing the same, and an anticancer drug containing the same

The present invention relates to a diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate derivative which induces cell apoptosis, a method of manufacturing the same, and an anti-cancer drug containing the same. A compound represented by chemical form

Synthetic diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates induce apoptosis

Background: The Hantzsch ester, diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, has been used as a hydride donor and its various biological effects have been reported. To identify chemotherapeutic agents with apoptotic effects, 21 diethyl 2,6-