5767-53-3

Basic information

• Product Name: 2,2'-(1,3-Propanediyl)bis(nitrilomethylidyne)bis(6-methoxyphenol)
• Synonyms: 2,2'-(1,3-Propanediyl)bis(nitrilomethylidyne)bis(6-methoxyphenol);2,2'-[1,3-Propanediylbis(nitrilomethylidyne)]bis(6-methoxyphenol);2,2'-[Trimethylenebis(nitrilomethylidyne)]bis(6-methoxyphenol);6,6'-[Trimethylenebis(nitrilomethylidyne)]bis(2-methoxyphenol);N,N'-Bis(2-hydroxy-3-methoxybenzylidene)-1,3-propanediamine;N,N'-Bis(3-methoxysalicylidene)trimethylenediamine
• CAS NO: 5767-53-3
• Molecular Formula: C₁₉H₂₂N₂O₄
• Molecular Weight: 342.389
• Mol File: 5767-53-3.mol
• Article Data: 35

Chemical Properties

• Boiling Point: 542°Cat760mmHg
• Flash Point: 281.6°C
• Appearance: /
• Density: 1.15g/cm³
• Vapor Pressure: 1.8E-13mmHg at 25°C
• Refractive Index: 1.586
• CAS DataBase Reference: 2,2'-(1,3-Propanediyl)bis(nitrilomethylidyne)bis(6-methoxyphenol)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-(1,3-Propanediyl)bis(nitrilomethylidyne)bis(6-methoxyphenol)(5767-53-3)
• EPA Substance Registry System: 2,2'-(1,3-Propanediyl)bis(nitrilomethylidyne)bis(6-methoxyphenol)(5767-53-3)

Safety Data

• Hazardous Substances Data: 5767-53-3(Hazardous Substances Data)

Usage

Type of compound

Bisphenol derivative

Uses

Production of industrial and consumer products (e.g. plastics, adhesives), antioxidant properties (stabilizer in polymers and coatings), production of certain pharmaceuticals

Safety

Relatively safe for use in specified applications, but proper handling and disposal procedures should be followed to minimize potential impact on human health and the environment.

InChI:InChI=1/C19H22N2O4/c1-24-16-8-3-6-14(18(16)22)12-20-10-5-11-21-13-15-7-4-9-17(25-2)19(15)23/h3-4,6-9,12-13,20-21H,5,10-11H2,1-2H3/b14-12+,15-13u

Upstream product

• 672-13-9 2-hydroxy-5-methoxybenzaldehyde 
• 109-76-2 Trimethylenediamine 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 

Downstream Products

• 774167-08-7 Mn(C₁₉H₂₀N₂O₄)(OCOCH₂C₆H₅)(H₂O) 
• 5767-55-5 2,2'-[propane-1,3-diylbis(iminomethylene)]bis(6-methoxyphenol) 
• 251324-68-2 diphenyl[N,N'-bis(3-methoxysalicaldehyde)-1,3-propylenediiminato]tin(IV) 
• 22523-89-3 {NiOC₆H₃(3-OCH₃)CHN(CH₂)3NCHC₆H₃(3-OCH₃)} 

Relevant articles and documents

Unprecedented photosensitivity of heterotrimetallic copper(ii)/sodium/mercury(ii) coordination polymer based thin film semiconductor device

A hetero-polynuclear complex, [{CuLNa}2(μ-1,1,3-NCS)HgCl(μ-Cl)(μ-1,3-NCS)]n {H2L = N,N′-bis(3-methoxysalicylidene)propane-1,3-diamine}, has been synthesized and characterized. The estimated optical ba

A new end-on (μ1,1) azido bridged [Zn2(L)2(Na)N3]n 1D chain derived from a trinuclear zinc complex: syntheses, crystal structures, photoluminescence properties and DFT study

A bicompartmental N2O4 donor symmetric Schiff base ligand has been deployed to synthesize a trinuclear zinc complex [Zn3(L)2Cl2], which upon treatment with sodium azide produces a new μ1,1-

Anion mediated diversity in the H-bonded assembly of a series of heteronuclear copper(II)/sodium(I) compounds

Three heteronuclear Cu(II)/Na(I) compounds, [Cu(vanpn)Na(NO 3)(H2O)] (1), [Cu(vanpn)Na(N3)(CH 3OH)] (2) and [Cu(vanpn)Na(NCS)(H2O)] (3) where H 2vanpn = N,N′-(1,3-propylene)-bis(3-methoxysa

Exploration of unconventional π-hole and C-H?H-C types of supramolecular interactions in a trinuclear Cd(ii) and a heteronuclear Cd(ii)-Ni(ii) complex and experimental evidence for preferential site selection of the ligand by 3d and 4d metal ions

In this present work we report the synthesis and structural characterisation of a trinuclear cadmium(ii) (1) and a di(phenoxido)-bridged dinuclear cadmium(ii)-nickel(ii) (2) complex derived from a bicompartmental (N2O4) Schiff base l

Preparation, crystal structures, and magnetic features for a series of dinuclear [NiIILnIII] schiff-base complexes: Evidence for slow relaxation of the magnetization for the DyIII derivative

A series of dinuclear [NiIILnIII] Schiff-base complexes (using a Schiff-base dicompartmental ligand derived from o-vanillin [H2valpn = 1,3-propanediylbis(2-iminomethylene-6-methoxy-phenol)]) with Ln = La, Ce, Pr, Nd, Sm, E

Design and catalytic studies of structural and functional models of the catechol oxidase enzyme

Abstract: The catechol oxidase activity of three copper/bicompartmental salen derivatives has been studied. One mononuclear, [CuL] (1), one homometallic, [Cu2L(NO3)2] (2), and one heterometallic, [CuMnL(NO3)sub

Structure, bonding, and catalytic activity of monodisperse, transition-metal-substituted CeO2 nanoparticles

We present a simple and generalizable synthetic route toward phase-pure, monodisperse transition-metal-substituted ceria nanoparticles (M0.1Ce0.9O2-x, M = Mn, Fe, Co, Ni, Cu). The solution-based pyrolysis of a series of he

Synthesis, X-ray crystal structure, photo luminescent property, antimicrobial activities and DFT computational study of Zn(II) coordination polymer derived from multisite N,O donor Schiff base ligand (H2L1)

A unique thiocyanato linked 1D chain of Zn(II) coordination polymer [Zn2L1(μ1,3-SCN)(η1SCN)]n (1) has been synthesized using potential multisite compartmental N,O donor Schiff base blocker ligand (Ls

3d-4f magnetic exchange interactions and anisotropy in a series of heterobimetallic vanadium(iv)-lanthanide(iii) Schiff base complexes

A series of heterobimetallic LnIII-VIVcompounds [Ln(VO)L(NO3)3(H2O)] (Ln = Gd(1), Tb(2), Dy(3), and Er(4)) assembled by a Schiff base ligand (H2L =N,N′-bis(1-hydroxy-2-benzylidene-6-methoxy

A rare flattened tetrahedral Mn(II) salen type complex: Synthesis, crystal structure, biomimetic catalysis and DFT study

A new flattened tetrahedral high spin Mn(II) complex (1) has been synthesized using N2O4 donor Schiff base ligand. Complex 1 was characterized by X-ray diffraction and various spectroscopic techniques. For further understanding of el