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The chemical compound "4-methyl-6-{[(2-{[(Z)-(3-methyl-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino}ethyl)amino]methylidene}cyclohexa-2,4-dien-1-one" is a complex organic molecule with a molecular formula of C18H20N2O2. It features a cyclohexa-2,4-dien-1-one core structure, with a methyl group at the 4th position and a 6-oxo group. The molecule also contains a Z-configured (3-methyl-6-oxocyclohexa-2,4-dien-1-ylidene)methyl group, which is connected to an aminoethyl chain that further links to another aminoethyl group. This intricate arrangement of functional groups and carbon atoms gives the compound its unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

6943-13-1

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6943-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6943-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6943-13:
(6*6)+(5*9)+(4*4)+(3*3)+(2*1)+(1*3)=111
111 % 10 = 1
So 6943-13-1 is a valid CAS Registry Number.

6943-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (6Z)-4-methyl-6-[[2-[[(Z)-(3-methyl-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino]ethylamino]methylidene]cyclohexa-2,4-dien-1-one

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:6943-13-1 SDS

6943-13-1Downstream Products

6943-13-1Relevant academic research and scientific papers

Synthesis, crystal structure and antimicrobial activity of a hetero trinuclear manganese(III)-iron(II) complex derived from N,N'-bis(5-methylsalicylidene)-1,2-diaminoethane

Hu, Xiao-Ming,Xue, Ling-Wei,Zhao, Gan-Qing,Yang, Wei-Chun

, p. 407 - 413 (2015)

A new hetero trinuclear manganese(III)-iron(II) complex, [Mn(salen)(H2O)]2[Fe(CN)6], in which salen is the dianionic form of N,N'-bis(5-methylsalicylidene)-1,2-diaminoethane, has been prepared and characterized by elementa

Synthesis and crystal structures of N,N'-bis(5-methylsalicylidene)ethane-1,2-diamine and its bromido-, phenolato-, and dicyanoamido-cobridged polymeric copper(II) complex

Qiu,Gu,Li,Xian,You,Zhu

, p. 331 - 337 (2017)

A bis-Schiff base N,N'-bis(5-methylsalicylidene)ethane-1,2-diamine (H2L) was prepared and characterized by elemental analysis, 1H NMR and 13C NMR spectra, MS, and single crystal X-ray diffraction (CIF file CCDC no. 1022761

Synthesis, Structure, and Catalytic Epoxidation Property of a New Phenolato and μ1,1,3-Azido Co-Bridged Polynuclear Manganese(III) Complex Derived from N,N′-Bis(5-methylsalicylidene)ethane-1,2-diamine

Wang, Ning

, p. 1434 - 1437 (2015)

A new phenolato and 1,1,3-azido co-bridged polynuclear manganese(iii) complex has been synthesised and characterised. The structure of the complex has been confirmed by single crystal X-ray diffraction analyses. The ability of the complex to catalyse the

Improving the single-molecule magnet properties of two pentagonal bipyramidal Dy3+compounds by the introduction of both electron-withdrawing and -donating groups

Dong, Yubao,Li, Dongfeng,Ma, Pengtao,Yin, Bing,Zhu, Li

, p. 12607 - 12618 (2021)

Two mononuclear Dy3+compounds [Dy(bmbpen-F)X] (X = Cl,1; Br,2) with a pentagonal bipyramidal (PBP) geometry were obtained fromN,N′-bis-(5-methyl-2-hydroxybenzyl)-N,N′-bis(5-fluoro-2-methylpyridyl)ethylenediamine (H2bmbpen-F) and dysp

Influences of polarizability effect of alkyl group and homoring competition effect of substituents on the NMR spectra of salen-type Schiff base

Wei, Bai-ying,Cao, Chen-zhong,Cao, Chao-tun

, p. 701 - 712 (2021/02/12)

Salen-type Schiff bases are a kind of important compounds and are widely used. In order to explore the effect of alkyl groups and substituents attached to aromatic ring on the chemical shifts, 63 title compounds were synthesized. Their 1H NMR and 13C NMR spectra were obtained; and the effects of the alkyl chain length and substituents on the chemical shifts (δH(CH=N), δC(CH=N), δH(OH), and δC(C-OH)) were studied. The results show that (1) the alkyl polarizability effect index (PEI) has an important influence on the chemical shifts of the above four atoms, with the increase of PEI, the values of δH(CH=N) and δc(CH=N) decrease, and the values of δH(OH) and δC(C-OH) increase. (2) The influence of substituent X attached to aromatic ring on the chemical shift is related to its position by taking OH or CH=N as reference. As for the effect of substituent on the chemical shifts, the effect of Hammett constant σ(X)-OH and excited-state substituent parameter (Formula presented.) with OH as reference are different from that ofσ(X)-CH=N and (Formula presented.) with CH=N as reference, and there is a “homoring competition effect” of the substituent. (3) The effect of the cross-interaction between X and OH on the chemical shift is also significantly different due to the different position of X. Quantitative correlation equations against chemical shifts were built for the four atoms, and the stability and prediction ability of the obtained equations were confirmed by leave-one-out cross validation.

Alteration of electronic effect causes change in rate determining step: Oxovanadium(IV)–salen catalyzed sulfoxidation of phenylmercaptoacetic acids by hydrogen peroxide

Kavitha,Subramaniam

, (2019/11/13)

Sulfoxidation of a series of phenylmercaptoacetic acids (PMAA) by hydrogen peroxide catalysed by oxovanadium(IV)–salen complexes has been carried out spectrophotometrically in 100% acetonitrile medium. The formation and involvement of hydroperoxovanadium(

Nickel(II) Complexes Derived from Bis-Schiff Bases: Synthesis, Crystal Structures, and Antimicrobial Activity

Han, Y. J.,Luo, X. Q.,Xue, L. W.

, p. 145 - 151 (2020/03/26)

Abstract: Nickel(II) complexes derived from the bis-Schiff bases N,N'-bis(5-methylsalicylidene)-1,2-diaminocyclohexane (H2La), N,N'-bis(5-methylsalicylidene)-1,2-diaminoethane (H2Lb) and N,N’-bis(3,5-difluorosal

Solvent-Dependent Bending Ability of Salen-Derived Organic Crystals

Kusumoto, Sotaro,Saso, Akira,Ohmagari, Hitomi,Hasegawa, Miki,Kim, Yang,Nakamura, Masaaki,Lindoy, Leonard F.,Hayami, Shinya

, p. 1692 - 1696 (2020/07/04)

The formation of plastic or brittle organic crystals of salen derivatives that depend on the solvents employed for crystallization is demonstrated. Large yellow crystals (ranging from mm to cm size) of ten different salen derivatives were obtained and inv

Excess axial electrostatic repulsion as a criterion for pentagonal bipyramidal DyIII single-ion magnets with high: U eff and T B

Jiang, Zhijie,Sun, Lin,Yang, Qi,Yin, Bing,Ke, Hongshan,Han, Jing,Wei, Qing,Xie, Gang,Chen, Sanping

, p. 4273 - 4280 (2018/04/26)

In this work, a large excess of electrostatic repulsion, arising from the axial ligands, over that from the equatorial ligands is taken as the design strategy for high performance pentagonal bipyramidal (PBP) DyIII single-ion magnets (SIMs). In

Synthesis, X-ray crystal structures, and antibacterial activities of Schiff base nickel(II) complexes with similar tetradentate Schiff bases

Xu,Xue,Wang

, p. 314 - 319 (2017/05/10)

Two new mononuclear complexes, [NiL1] · CH3OH (I) and [NiL2] (II), have been prepared from the tetradentate Schiff bases N,N'-bis(5-methylsalicylidene)ethylenediamine (H2L1) and N,N'-bis(5-methylsalic

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