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Phenol, 4-[(2-pyridinylimino)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73447-08-2

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73447-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73447-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,4 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73447-08:
(7*7)+(6*3)+(5*4)+(4*4)+(3*7)+(2*0)+(1*8)=132
132 % 10 = 2
So 73447-08-2 is a valid CAS Registry Number.

73447-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(pyridin-2-ylamino)methylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-N-[4-hydroxybenzalidene]aminopyridine

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:73447-08-2 SDS

73447-08-2Downstream Products

73447-08-2Relevant academic research and scientific papers

Annulation of Conjugated Azine-Imine with a Sulfoxonium Ylide in a Noncarbenoid Route to Synthesize Multisubstituted Imidazole-Fused Heterocycles

Guchhait, Sankar K.,Saini, Meenu,Khivsara, Viren J.,Giri, Santosh K.

, p. 5380 - 5387 (2021/05/05)

A new [4+1]-annulation of in situ generated heterocyclic azine-aldimines with β-keto sulfoxonium ylides has been developed. The reaction constructs N-fused imidazole rings. In the reaction, the ylides play a dual-functional role of a nucleophilic 1,1-dipo

A novel approach towards design, synthesis and evaluation of some Schiff base analogues of 2-aminopyridine and 2-aminobezothiazole against hepatocellular carcinoma

Chacko, Shinu,Samanta, Subir

, p. 162 - 176 (2017/02/26)

Hepatocellular carcinoma is the most common primary malignancy of the liver with poor prognosis. In this study novel, Schiff's bases of 2-aminopyridine (SSSC-26 to 31) and 2-aminobenzothiazole (SSSC-32 to 37) were designed, synthesised and evaluated for antioxidant potential using DPPH method, and anti-hepatocellular carcinoma property using diethylnitrosamine (DEN) induced hepatocellular carcinoma rat model. The in-silico pharmacokinetic, rule of five and toxicity studies reveals that all the leads have an excellent intrinsic quality and sufficient structural features necessary for an oral activity. Molecular docking studies of all compounds into the ligand binding pocket of checkpoint kinase1 and vascular endothelial growth factor receptor-2 was also performed using Schrodinger software suite v8.5, and which have shown good Glide scores. Further compounds were synthesised based on the docking score and ADMET profile. The 1,1-diphenyl-2-picrylhydrazil (DPPH) scavenging study was carried out, and results showed that SSSC-29 (IC50-63.60) and SSSC-33 (IC50-60.32) were having good anti-oxidant potential in comparison with ascorbic acid (IC50-55.27). SSSC-33 further evaluated for anti-cancer potential against diethylnitrosamine (200 mg/kg bw) induced hepatocellular carcinoma in rats. The biochemical, histopathological and morphological data showed that SSSC-33 can reverse the changes occurred in the cancerous liver significantly. All these findings suggested that SSSC-33-((benzo[d]thiazol-2-ylimino) methyl)phenol) could be a potential compound in combating the oxidative damage of hepatic cells occurred due to the development of hepatocellular carcinoma induced by a chemical carcinogen, DEN.

Theoretical vibrational mode analysis of schiff bases using semi empirical methods-II

Agnihotri, Sonal,Singh, Bhoop,Burman, Kiran,Arora, Kishor

experimental part, p. 2089 - 2091 (2012/02/14)

Two new Schiff bases viz., 2N-[(4-chlorobenzalidene)aminopyridine] and 2N-[(4-hydroxybenzalidene)aminopyridine] were synthesized using 4-chlorobenzaldehyde, 4-hydroxybenzaldehyde and 2-amino pyridine in separate procedures. Their IR spectra was obtained e

Physicochemical investigations of Th(IV) and UO2(VI) complexes with new schiff bases along with their toxic effects

Agnihotri, Sonal,Arora, Kishor

body text, p. 1045 - 1054 (2011/12/14)

Schiff bases were obtained using p-trimethoxy benzaldehyde, p-hydroxyl benzaldehyde and 2-amino pyridine to prepare new complexes of thorium(IV) and dioxouranium(VI) metals by various anions. The synthesized ligands and complexes were analytically studied

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