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dimethyl 4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56820-24-7

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56820-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56820-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56820-24:
(7*5)+(6*6)+(5*8)+(4*2)+(3*0)+(2*2)+(1*4)=127
127 % 10 = 7
So 56820-24-7 is a valid CAS Registry Number.

56820-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3,5-dimethoxycarbonyl-4-phenyl-1,4-dihydropyridine

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:56820-24-7 SDS

56820-24-7Relevant academic research and scientific papers

Photodimerization of 4-Aryl-1,4-dihydropyridines in 1-Butyl-3-methylimidazolium tetrafluoroborate

He, Jing-Yu,Jia, Hui-Zhen,Yao, Qing-Guo,Liu, Si-Jie,Yue, Hong-Kun,Liu, Wei-Yan,Wang, Xiao-Hong,Tian, Jing-Chao

, p. 1596 - 1598 (2014)

A simple, efficient, and convenient method for the photodimerization of 4-aryl-1,4-dihydropyridine in room-temperature ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([Bmim][BF4]) has been developed. By this way, head-to-tail syn-di

A Cofactor-Substrate-Based Supramolecular Fluorescent Probe for the Ultrafast Detection of Nitroreductase under Hypoxic Conditions

Duan, Chunying,Gao, Xu,Jiao, Yang,Si, Wen,Zhang, Lei

supporting information, p. 6021 - 6027 (2020/03/04)

Identifying the location and expression levels of enzymes under hypoxic conditions in cancer cells is vital in early-stage cancer diagnosis and monitoring. By encapsulating a fluorescent substrate, L-NO2, within the NADH mimic-containing metal–organic capsule Zn-MPB, we developed a cofactor-substrate-based supramolecular luminescent probe for ultrafast detection of hypoxia-related enzymes in solution in vitro and in vivo. The host–guest structure fuses the coenzyme and substrate into one supramolecular probe to avoid control by NADH, switching the catalytic process of nitroreductase from a double-substrate mechanism to a single-substrate one. This probe promotes enzyme efficiency by altering the substrate catalytic process and enhances the electron transfer efficiency through an intra-molecular pathway with increased activity. The enzyme content and fluorescence intensity showed a linear relationship and equilibrium was obtained in seconds, showing potential for early tumor diagnosis, biomimetic catalysis, and prodrug activation.

Ultrasound-mediated synthesis of 4-substituted 1,4-dihydropyridine-3,5- dicarboxylates catalyzed by 1-carboxymethyl-3-methylimidazolium tetrafluoroborate under solvent free condition

He, Jing-Yu,Jia, Hui-Zhen,Yao, Qing-Guo,Liu, Si-Jie,Yue, Hong-Kun,Yu, Hong-Wei,Hu, Rui-Sheng

, p. 144 - 148 (2014/12/09)

4-Substituted 1,4-dihydropyridine-3,5-dicarboxylates (4) have been synthesized by the solvent-free reaction of aldehyde, methyl propiolate and ammonium carbonate catalyzed by ionic liquid 1-carboxymethyl-3-methylimidazolium tetrafluoroborate under ultraso

Synthesis of 3-5-diacyl-4-phenyl-1,4-dihydropyridines

Bennasar, M.-Lluisa,Juan, Cecilia,Bosch, Joan

, p. 9275 - 9278 (2007/10/03)

3,5-Diacyl-4-phenyl-1,4-dihydropyridines have been synthesized via a regio- and chemoselective addition of Ph2Cu(CN)Li2 to β-substituted N- alkylpyridinium salts, followed by acylation of the intermediate 1,4- dihydropyridines with t

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