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N-(4-Chlorophenyl)-3-pyridylmethyleneamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41855-64-5

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41855-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41855-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,5 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41855-64:
(7*4)+(6*1)+(5*8)+(4*5)+(3*5)+(2*6)+(1*4)=125
125 % 10 = 5
So 41855-64-5 is a valid CAS Registry Number.

41855-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-chlorophenyl)-1-pyridin-3-ylmethanimine

1.2 Other means of identification

Product number -
Other names -

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:41855-64-5 SDS

41855-64-5Relevant academic research and scientific papers

Fluorodynamers Displaying Tunable Fluorescence on Constitutional Exchanges in Solution and at Solid Film–Solution Interface

Si, Mingran,Zhu, Weijia,Zhang, Yan,Barboiu, Mihail,Chen, Jinghua

supporting information, p. 10191 - 10194 (2020/07/13)

Dynamic covalent polymers—dynamers—are adaptive materials that offer timely variant adaptive macroscopic organization across extended scales. In the current study, imine exchange reactions and fluorescence transfer can occur at the interfaces between vari

Diverse C-6 substituted 4-methyl-2-(2-, 3- and 4-pyridinyl)quinolines: synthesis, in vitro anticancer evaluation and in silico studies

Kouznetsov, Vladimir V.,Robles-Castellanos, Mayra L.,Sojo, Felipe,Rojas-Ruiz, Fernando A.,Arvelo, Francisco

, p. 551 - 561 (2017/02/15)

A series of twelve 4-methyl-2-(2-, 3- and 4-pyridinyl)quinolines 7–9 was synthesized using modified Kametani reaction protocol and their in vitro cytotoxicity was tested against human cancer cell lines MCF-7, SKBR-3, PC3, HeLa, comparing with human dermis

Development of novel vitamin D receptor-coactivator inhibitors

Sidhu, Preetpal S.,Nassif, Nicholas,McCallum, Megan M.,Teske, Kelly,Feleke, Belaynesh,Yuan, Nina Y.,Nandhikonda, Premchendar,Cook, James M.,Singh, Rakesh K.,Bikle, Daniel D.,Arnold, Leggy A.

supporting information, p. 199 - 204 (2014/03/21)

Nuclear receptor coregulators are master regulators of transcription and selectively interact with the vitamin D receptor (VDR) to modulate cell differentiation, cell proliferation, and calcium homeostasis. Herein, we report the syntheses and evaluation of highly potent and selective VDR-coactivator inhibitors based on a recently identified 3-indolylmethanamine scaffold. The most active compound, PS121912, selectively inhibited VDR-mediated transcription among eight other nuclear receptors tested. PS121912 is also selectively disrupting the binding between VDR and the third nuclear receptor interaction domain of the coactivator SRC2. Genetic studies revealed that PS121912 behaves like a VDR antagonist by repressing 1,25-(OH)2D3 activated gene transcription. In addition, PS121912 induced apoptosis in HL-60.

Aqueous extract of the pericarp of Sapindus trifoliatus fruits: A novel 'green' catalyst for the aldimine synthesis

Pore, Santosh,Rashinkar, Gajanan,Mote, Kavita,Salunkhe, Rajeshri

experimental part, p. 1796 - 1800 (2011/08/05)

The catalytic efficiency in organic synthesis of the aqueous extract of the pericarp of Sapindus trifoliatus fruits was evaluated. The synthesis of a series of aldimines from aromatic aldehydes and amines was successfully catalyzed by the extract, whereas aromatic ketones and amines did not yield ketimines under comparable reaction conditions, indicating the chemoselective catalysis of the extract. The catalytic activity of the extract is due to saponins, which have a common structural skeleton containing a pentacyclic triterpenoid part substituted with different carbohydrate side chains. The mild conditions, high yields, and short reaction times not only make this protocol a valuable alternative to the conventional methods, but it also becomes significant under the roof of environmentally greener and safer processes.

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