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1258669-34-9

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1258669-34-9 Usage

Type of compound

Synthetic dye.

Usage

Commonly used as a colorant and pigment in various industrial applications, such as plastics, textiles, and ink.

Chemical structure

Two benzene rings linked by a diazenediylbis group, with two nitrile and two phenyl functional groups attached.

Color

Vibrant red.

Stability

High stability, resistance to fading and degradation.

Environmental and health impacts

Potential concerns have been raised, and some applications have been regulated or restricted in certain regions.

Check Digit Verification of cas no

The CAS Registry Mumber 1258669-34-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,6,6 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1258669-34:
(9*1)+(8*2)+(7*5)+(6*8)+(5*6)+(4*6)+(3*9)+(2*3)+(1*4)=199
199 % 10 = 9
So 1258669-34-9 is a valid CAS Registry Number.

1258669-34-9 Well-known Company Product Price

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  • Sigma-Aldrich

  • (43359)  Manganese(II) ionophore II  Selectophore, function tested

  • 1258669-34-9

  • 43359-50MG

  • 2,357.55CNY

  • Detail

1258669-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[[2-[[2-[(6-oxocyclohexa-2,4-dien-1-ylidene)methylamino]phenyl]diazenyl]anilino]methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,2'-(((Diazene-1,2-diylbis(2,1-phenylene))bis(azanylylidene))bis(methanylylidene))diphenol

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:1258669-34-9 SDS

1258669-34-9Downstream Products

1258669-34-9Relevant articles and documents

Synthesis, characterization, spectral and catalytic activity of tetradentate (NNNO) azo-imine Schiff base copper(II) complexes

Pratihar, Jahar Lal,Mandal, Paritosh,Brand?o, Paula,Mal, Dasarath,Felix, Vitor

, p. 221 - 228 (2018)

The hexadentate ligand, 2,2′-bis(salicylideneamino)azobenzene, 1 has been synthesized from 2,2′-diaminoazobenzene and salicylaldehyde in refluxing diethyl ether. Reaction of ligand 1 with Cu(II) acetate and Cu(II) perchlorate separately in methanol afforded tetradentate (N,N,N,O) Cu(II) complexes, Cu(L) & [Cu(HL)]ClO4 respectively [where H2L represent the one imine moiety cleavage product of ligand 1 (H represents the dissociable amino and phenolic protons)]. These were characterized by microanalytical data and spectroscopic studies. In addition, the crystal structures of the ligand 1 and complexes Cu(L) & [Cu(HL)]ClO4 were determined by X-ray diffraction analysis. The diffraction analysis revealed that the ligand (H2L) binds Cu(II) centers in (N,N,N,O) tetra dentate fashion in distorted square planer geometry. In complex [Cu(HL)]ClO4 the apical position of copper center is weakly coordinated with one perchlorate ion. The dimeric structure of the molecule [Cu(HL)]ClO4 is stabilized through NH2···O hydrogen bonds. The fluorescence and redox property of ligand 1 and complexes Cu(L) & [Cu(HL)]ClO4 were studied. Preliminary DFT calculations were carried out using crystallographic coordinates to understand the electronic spectra and redox properties of the ligand and complexes. The complex Cu(L) shows very good catalytic activities towards oxidation of benzyl alcohol to benzaldeyhde (under solvent-free condition) and organic thioethers to sulfoxide and sulfones using H2O2 as the oxidant.

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