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

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  • 53219-32-2 Structure
  • Basic information

    1. Product Name: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(2-methylphenyl)-, diethyl ester
    2. Synonyms:
    3. CAS NO:53219-32-2
    4. Molecular Formula: C20H25NO4
    5. Molecular Weight: 343.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53219-32-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(2-methylphenyl)-, diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(2-methylphenyl)-, diethyl ester(53219-32-2)
    11. EPA Substance Registry System: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(2-methylphenyl)-, diethyl ester(53219-32-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 53219-32-2(Hazardous Substances Data)

53219-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53219-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,1 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53219-32:
(7*5)+(6*3)+(5*2)+(4*1)+(3*9)+(2*3)+(1*2)=102
102 % 10 = 2
So 53219-32-2 is a valid CAS Registry Number.

53219-32-2SDS

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-o-tolyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester

1.2 Other means of identification

Product number -
Other names 2,6-Dimethyl-4-o-tolyl-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:53219-32-2 SDS

53219-32-2Relevant articles and documents

Ferric Sulfasalazine Sulfa Drug Complex Supported on Cobalt Ferrite Cellulose; Evaluation of Its Activity in MCRs

Rostamizadeh, Shahnaz,Daneshfar, Zahra,Khazaei, Ali

, p. 2091 - 2114 (2020/01/31)

Abstract: The green and nano catalyst was simply prepared through the reaction of ferric sulfasalazine with nanomaterial CoFe2O4-cellulose as a magnetic biopolymer surface. This novel heterogeneous organometallic catalyst was charact

Intermolecular [2 + 2] Cycloaddition of 1,4-Dihydropyridines with Olefins via Energy Transfer

Wang, Chengfeng,Lu, Zhan

supporting information, p. 5888 - 5891 (2017/11/10)

A highly regio- and diastereoselective visible-light-promoted [2 + 2] cycloaddition between readily available 1,4-dihydropyridines and olefins has been developed. This strategy is operationally simple and atom-economical and enables the construction of strained polysubstituted 2-azabicyclo[4.2.0]octanes with three all-carbon quaternary centers with good functional group tolerance. These products can be easily converted to various structurally unique derivatives. The primary mechanistic studies demonstrated that the reaction proceeds through an energy transfer pathway.

Sulfated zirconia-catalyzed synthesis of 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) under solventless conditions: Competitive multicomponent Biginelli vs. Hantzsch reactions

Angeles-Beltran, Deyanira,Lomas-Romero, Leticia,Lara-Corona, Victor H.,Gonzalez-Zamora, Eduardo,Negron-Silva, Guillermo

, p. 731 - 738 (2007/10/03)

The catalytic ability of ZrO2/SO42- to promote solventless three-component condensation reactions of a diversity of aromatic aldehydes, urea or thoiurea and ethyl acetoacetate was studied. Products resulting from Hantzsch

An efficient and fast procedure for the Hantzsch dihydropyridine synthesis under microwave conditions

?hberg,Westman

, p. 1296 - 1298 (2007/10/03)

Abstract: A single-mode microwave cavity synthesizer with temperature and pressure control was used to accelerate the Hantzsch synthesis of 4-aryl and 4-alkyl-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylates. In comparison with both conventional method

Process for 1,4-dihydropyridine compounds using a titanamine catalyst

-

, (2008/06/13)

A process for the preparation of 1,4-dihydropyridine compounds, especially N-substituted 1,4-dihydropyridine compounds, is disclosed. The compounds are useful as cardiovascular agents and also as starting materials for the preparation of certain cyclized compounds which have properties as calcium entry blockers.

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