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The chemical compound "4-[[2-[(4-oxo-1-cyclohexa-2,5-dienylidene)methylamino]ethylamino]methylidene]cyclohexa-2,5-dien-1-one" is a complex organic molecule with a molecular formula of C16H17NO2. It features a cyclohexa-2,5-dien-1-one core structure, which is a derivative of cyclohexadienone, with a 4-oxo group indicating the presence of a carbonyl group at the 4-position. The molecule also contains a series of nitrogen-containing groups, including a methylamino group attached to the cyclohexadienyl ring, and an additional ethylamino group that forms a bridge between two carbon atoms of the ring. 4-[[2-[(4-oxo-1-cyclohexa-2,5-dienylidene)methylamino]ethylamino]methylidene]cyclohexa-2,5-dien-1-one is characterized by its conjugated diene system and the presence of multiple nitrogen atoms, which can contribute to its reactivity and potential applications in various chemical processes.

5340-13-6

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5340-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5340-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5340-13:
(6*5)+(5*3)+(4*4)+(3*0)+(2*1)+(1*3)=66
66 % 10 = 6
So 5340-13-6 is a valid CAS Registry Number.

5340-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[2-[(4-oxocyclohexa-2,5-dien-1-ylidene)methylamino]ethylamino]methylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names N,N'-bis-(4-hydroxy-benzyliden)-ethylenediamine

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:5340-13-6 SDS

5340-13-6Relevant academic research and scientific papers

Synthesis and Characterization of Poly(urethane-ether azomethine) Fatty Amide Based Corrosion Resistant Coatings from Pongamia glabra Oil: An Eco-Friendly Approach

Alam, Manawwer,Alandis, Naser M.,Ahmad, Naushad,Naushad, Mu

, (2016)

A novel attempt has been made to incorporate azomethine group in the backbone of polyurethane ether Pongamia oil fatty amide. The overall reaction was carried out in different steps like preparation of N,N-bis(2-hydroxyethyl) Pongamia glabra oil fatty ami

Synthesis, characterization and biological evaluation of ferrocene based poly(azomethene)esters

Gul, Asghari,Sarfraz, Sehrish,Akhter, Zareen,Siddiq, Muhammad,Kalsoom, Saima,Perveen, Fouzia,Ansari, Farzana Latif,Mirza, Bushra

, p. 91 - 99 (2015)

A new ferrocene containing poly(azomethine)ester (PFe) was synthesized by polycondensation of a preformed 4-((2-(4hydroxybenzylideneamino)ethylimino)methyl)phenol, (SB) and 1,1′-ferrocenyl dicarbonyl chloride. Various aliphatic and aromatic sequences (1,3

One-pot synthesis of imidazolinium salts via the ring opening of tetrahydrofuran

Huang, Yong-Qing,Zhao, Yue,Wang, Peng,Okamura, Taka-Aki,Laforteza, Brian N.,Lu, Yi,Sun, Wei-Yin,Yu, Jin-Quan

supporting information, p. 12430 - 12433 (2017/10/06)

A new one-pot synthesis of C2-hydroxypropyl-substituted imidazolinium salts via the ring opening of tetrahydrofuran (THF) with N,N′-disubstituted diamines has been developed. Preliminary studies of the reaction mechanism suggest the CO2-promoted oxidative ring opening of THF followed by Hg(ii)-mediated oxidation of an imidazolidine intermediate. These novel C2-substituted imidazolinium salts have shown to be active catalysts for the aza-Diels-Alder reactions.

Synthesis of new antifungal 1,2,4-bis-oxadiazolines using cycloaddition reaction of nitrile oxide with bis-Schiff base

Toumi, Ahmed,Daami-Remadi, Mejda,Jannet, Hichem Ben

, p. 922 - 928 (2013/08/15)

A series of arylaldehydes and acetophenone when treated with 1,2-ethanediamine afford the bis-Schiff bases N,N'- bis(arylidene)-ethane-l,2- diamines 1-8, N,N'-bis(arylmethylene)-ethane-l,2-diamines 9-10 and the N,N'-bis(l- phenylethylidene)-ethane-l,2-dia

Synthesis and biological evaluation of novel substituted-imidazolidine derivatives

Husain, Asif,Bhutani, Rubina,Kumar, Deepak,Shin, Dong-Soo

, p. 227 - 233 (2013/07/26)

A series of newer substituted-imidazolidine derivatives 3a-k were synthesized and assayed in vivo to investigate their anti-inflammatory, analgesic and antiulcer activity. The results of biological evaluation revealed that the three compounds, 4-[1,3-bis(4-hydroxy-3-methoxybenzyl)-2- imidazolidinyl]phenyldiethylamine (3g), 4-[1,3-bis(3-Ethoxy-4-hydroxybenzyl)-2- imidazolidinyl] phenyldiethylamine (3h) and 4-(1,3-bis(benzo[d][1,3]dioxol-5- ylmethyl)-4-methylimidazolidin-2-yl)-N,N-diethylbenzenamine (3j) were good in their anti-inflammatory and analgesic actions. Additionally these derivatives showed superior GI safety profile as compared to that of the standard drug in terms of low severity index. The results are statistically treated for its significance.

Preparation and characterization of new polyesters derived from schiff bases

Channar, Abdul Hamid,Sheikh, Abida Ali,Khuhawar, Muhammad Yar,Majidano, Subhan Ali,Pirzada, Tajnees

, p. 151 - 156 (2013/05/21)

Three polyesters have been prepared by the reaction of terephthaloyl chloride on Schiff bases derived from 4- hydroxybenzyldehyde and meso- stilbenediamine, ethylenediamine or 4- nitrophenylenediamine.The polymers were obtained in good yield (85% theoriti

FBXO3 INHIBITORS

-

Page/Page column 53, (2014/01/08)

The present application discloses benzathine and related compounds and their use as FBXO-3 inhibitors.

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