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14258-08-3

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14258-08-3 Usage

Chemical structure

1,4-Dihydro-1,2,4,6-tetramethyl-3,5-pyridinedicarboxylic acid diethyl ester

Functionality

Antioxidant and light stabilizer

Applications

a. Polymers, plastics, and coatings
b. Industrial products (adhesives, sealants, lubricants)
c. Agricultural industry (protection of crops and materials)

Purpose

To prevent degradation and deterioration caused by heat, light, and oxygen exposure

Benefits

Enhances stability and performance of products, protects crops and materials from oxidative damage

Consideration

Valuable additive in various industrial and agricultural processes

Check Digit Verification of cas no

The CAS Registry Mumber 14258-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,5 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14258-08:
(7*1)+(6*4)+(5*2)+(4*5)+(3*8)+(2*0)+(1*8)=93
93 % 10 = 3
So 14258-08-3 is a valid CAS Registry Number.

14258-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,6-tetramethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester

1.2 Other means of identification

Product number -
Other names 1,4-Dihydro-1,2,4,6-tetramethyl-pyridin-3,5-dicarbonsaeure-diethylester

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:14258-08-3 SDS

14258-08-3Relevant articles and documents

Intermolecular Aryne Ene Reaction of Hantzsch Esters: Stable Covalent Ene Adducts from a 1,4-Dihydropyridine Reaction

Trinchera, Piera,Sun, Weitao,Smith, Jane E.,Palomas, David,Crespo-Otero, Rachel,Jones, Christopher R.

supporting information, p. 4644 - 4647 (2017/09/12)

The reaction of arynes with 1,4-dihydropyridines affords 2-aryl-1,2-dihydropyridines or 2-methylene-3-aryl-1,2,3,4-tetrahydropyridines via a regioselective C-2 or C-3 arylation. These compounds are the first series of isolable and bench-stable covalent ene adducts formed between dihydropyridines and unsaturated substrates. Experimental studies and DFT calculations provide mechanistic support for a concerted intermolecular aryne ene process, which may have implications for NAD(P)H model reactions.

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