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2-(((2-(diethylamino)ethyl)imino)methyl)-6-methoxyphenol **2-(((2-(diethylamino)ethyl)imino)methyl)-6-methoxyphenol** is a Schiff base ligand that coordinates with metal ions (e.g., Co(III), Fe(III), Cd(II)) through its imine nitrogen and phenoxo oxygen atoms, often exhibiting zwitterionic behavior. It can act as a bi-, tri-, or tetradentate ligand depending on the metal complex, with its diethylaminoethyl side chain remaining pendant in some cases. This ligand has been used in synthesizing complexes with varied structural and magnetic properties, including catalytic activity in aerobic epoxidation and participation in supramolecular interactions.

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  • 1012369-02-6 Structure
  • Basic information

    1. Product Name: 2-(((2-(diethylamino)ethyl)imino)methyl)-6-methoxyphenol
    2. Synonyms: 2-(((2-(diethylamino)ethyl)imino)methyl)-6-methoxyphenol
    3. CAS NO:1012369-02-6
    4. Molecular Formula:
    5. Molecular Weight: 250.341
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1012369-02-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(((2-(diethylamino)ethyl)imino)methyl)-6-methoxyphenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(((2-(diethylamino)ethyl)imino)methyl)-6-methoxyphenol(1012369-02-6)
    11. EPA Substance Registry System: 2-(((2-(diethylamino)ethyl)imino)methyl)-6-methoxyphenol(1012369-02-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1012369-02-6(Hazardous Substances Data)

1012369-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1012369-02-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,2,3,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1012369-02:
(9*1)+(8*0)+(7*1)+(6*2)+(5*3)+(4*6)+(3*9)+(2*0)+(1*2)=96
96 % 10 = 6
So 1012369-02-6 is a valid CAS Registry Number.

1012369-02-6Downstream Products

1012369-02-6Relevant articles and documents

Azide/thiocyanate incorporated cobalt(III)-Schiff base complexes: Characterizations and catalytic activity in aerobic epoxidation of olefins

Shit, Shyamapada,Saha, Debraj,Saha, Dipankar,Guru Row, Tayur N.,Rizzoli, Corrado

, p. 103 - 110 (2014)

Reaction of cobalt(II) perchlorate hexahydrate with a potentially tetradentate Schiff base ligand, HL (2-methoxy-6-[(2-diethylaminoethylimino) methyl]phenol) in presence of sodium azide and sodium thiocyanate yields two complexes [Co(L)(HL)(N3)

Synthesis and characterization of three new photo-luminescent cadmium(II) complexes with azide: Variation in molecular structures with changes in the denticity of blocking ligands

Roy, Sumit,Bhaumik, Prasanta Kumar,Harms, Klaus,Chattopadhyay, Shouvik

, p. 155 - 161 (2015)

Three new cadmium(II) complexes, [Cd(dede)(μ-1,3-N3)(μ-1,1-N3)]n (1), [{Cd3(L1)2(μ-1,1-N3)4(CH3OH)2}·2CH3OH·2H2O]n/su

Synthesis, characterization and magnetic study of two new octahedral iron(III) complexes with pendant zwitterionic Schiff bases

Jana, Subrata,Bhattacharyya, Anik,Ghosh, Biswa Nath,Rissanen, Kari,Herrero, Santiago,Jiménez-Aparicio, Reyes,Chattopadhyay, Shouvik

, p. 715 - 723 (2016)

Two Schiff bases, HL1[2-((3-(dimethylamino)propylimino)methyl)-5-bromophenol] and HL2[2-((2-(diethylamino)ethylimino)methyl)-6-methoxyphenol], have been employed to prepare two new octahedral iron(III) complexes, [Fe(HL1)2(N3)2]ClO4·2H2O (1) and [Fe(HL2)2(NCS)2]ClO4·H2O (2). Both complexes are characterized by spectral and elemental analyses. Single crystal X-ray diffraction studies confirm their structures. In both complexes, Schiff bases are trapped in their zwitterionic forms and coordinated to iron(III) only through the imine nitrogen and phenoxo oxygen, i.e., they behave as bi-dentate ligands, keeping the remaining potential donor sites pendant. The measurement of χMvs. T for both complexes shows a continuous increase in susceptibility as the temperature decreases. The χM·T values from 300 to 2 K and the shape of these curves for both complexes discard the existence of a high-spin/low-spin transition. The decrease in χM·T of 1 with temperature is more pronounced than that expected for a complex with a small zero-field splitting. The magnetic behavior of 1 is explained by proposing the existence of a physical mixture of S = 5/2 and S = 1/2 spins and the presence of zero-field splitting in the S = 5/2 species.

A combined experimental and theoretical study on supramolecular assemblies in octahedral cobalt(III) salicylaldimine complexes having pendant side arms

Ghosh, Kousik,Banerjee, Abhisek,Roy, Sumit,Bauzá, Antonio,Frontera, Antonio,Chattopadhyay, Shouvik

, p. 86 - 95 (2016)

Two mononuclear cobalt(III) complexes, [Co(L1)(N3)2(deen)] (1) and [Co(L2)(N3)2(DMSO)] (2), where HL1 {2-(2-(diethylamino)ethyliminomethyl)-4-bromophenol} and HL2 {2-(2-(diethylamino)ethyliminomethyl)-6-methoxyphenol} are tridentate and tetradentate Schiff bases, respectively and deen is a bidentate chelating ligand, N,N-diethyl-1,2-diaminoethane, were prepared and characterized by elemental and spectral analysis. X-ray crystal structure determination confirmed their structures. Both complexes are meridional isomers. The solid state structures show the participation of the organic ligands in concurrent conventional and unconventional C-H. . .π interactions along with hydrogen bonding. The energetic features of these interactions have also been studied by means of DFT calculations.

Mono, di and trinuclear photo-luminescent cadmium(II) complexes with N2O and N2O2 donor salicylidimine Schiff bases: Synthesis, structure and self assembly

Roy, Sumit,Chattopadhyay, Shouvik

, p. 72 - 77 (2015)

Four new octahedral cadmium(II) complexes, [(Cd)(L1)(HL1)](ClO4) (1), [Cd2(L2)2(SCN)2(CH3OH)2] (2), [(CdL3)3(μ-1,1,1-OH)](ClO4/s

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