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Phenol, 2,2'-[1,2-ethanediylbis(nitrilomethylidyne)]bis[5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89130-15-4

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89130-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89130-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,3 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89130-15:
(7*8)+(6*9)+(5*1)+(4*3)+(3*0)+(2*1)+(1*5)=134
134 % 10 = 4
So 89130-15-4 is a valid CAS Registry Number.

89130-15-4SDS

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 bis-(4-methyl-salicylidene)-ethylenediamine

1.2 Other means of identification

Product number -
Other names Bis(4-methyl-salicyliden)-aethylendiamin

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:89130-15-4 SDS

89130-15-4Downstream Products

89130-15-4Relevant academic research and scientific papers

A novel series of CoIII(salen-type) complexes containing a seven-membered metallacycle: Synthesis, structural characterization and factors affecting the metallacyclization rate

Siega, Patrizia,Dreos, Renata,Brancatelli, Giovanna,Zangrando, Ennio,Tavagnacco, Claudio,Vrdoljak, Visnja,Hrenar, Tomica

, p. 909 - 920 (2014)

A series of electronically tuned trans-[CoIII(chel)(CH 2Cl)]2 complexes, where chel is a salen derivative (salen = 2,2′-ethylenebis(nitrilomethylidene)diphenol) containing either two or four methyl substituents in differen

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.

Nickel complexes as efficient catalysts in multicomponent synthesis of tetrahydropyridine derivatives

Yankin, Andrei N.,Dmitriev, Maksim V.

supporting information, p. 3481 - 3489 (2020/08/13)

Ni(Salen) complexes as an efficient, homogeneous catalysts revealed a catalytic activity toward the one-pot synthesis of tetrahydropyridine derivatives through the pseudo five-component reactions of aromatic aldehydes, aromatic amines, and β-ketoesters in ethanol at room temperature. Mild reaction conditions, good yields, high diastereoseletivity, operational simplicity, and the absence of tedious separation procedures, clean reaction profiles, high atom economy, inexpensive starting materials, and environmentally benign catalyst are the key advantages of the present MCRs protocol.

Chemosensor activity of 2-(anthracen-9-yl)-substituted imidazolidines and hexahydropyrimidines

Tolpygin

scheme or table, p. 104 - 108 (2012/05/20)

A number of 2-(anthracen-9-yl)-substituted imidazolidines and hexahydropyrimidines were synthesized by reaction of N,N'-bis[aryl(hetaryl) methyl]ethylene-1,2-diamines and N,N'-bis[aryl(hetaryl)methyl]-propane-1,3- diamines with anthracene-9-carbaldehyde. The obtained compounds showed chemosensor activity toward Cd2+, Cu2+, and Hg2+ ions. Pleiades Publishing, Ltd., 2012.

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