17954-12-0

Usage

Molecular Weight

256.26 g/mol

Physical State

Solid

Appearance

Pale yellow solid

Solubility

Slightly soluble in water, soluble in organic solvents like ethanol, acetone, and chloroform.

Functional Groups

Two aldehyde groups (-CHO), two hydroxyl groups (-OH), and a propane linking group (-CH2CH2CH2-).

Reactivity

Reacts with nucleophiles, electrophiles, and other organic compounds.

Uses

Production of polymers and resins, particularly in the manufacture of epoxy resins. Building block for the synthesis of specialty chemicals and pharmaceuticals. Applications in the production of adhesives, coatings, and composite materials.

Value in Industry

Unique structure and functional groups make it a valuable component in the chemical industry for the creation of a wide range of products.

Upstream product

• 90-02-8 salicylaldehyde 
• 109-64-8 1,3-dibromo-propane 
• 89-95-2 2-methyl-benzyl alcohol 
• 15886-84-7 1,3-dimesyloxypropane 
• 33838-32-3 potassium 2-formylphenolate 
• 90-01-7 salicylic alcohol 
• 142-28-9 1,3-Dichloropropane 

Downstream Products

• 122360-50-3 2,2'-propanediyldioxy-di-benzaldehyde bis-phenylimine 
• 141070-37-3 C₅₁H₄₈Cl₈N₄O₂ 
• 134777-68-7 C₂₅H₂₆N₆O₈ 
• 178384-04-8 3,23-diphenyl-12,13,27,28-tetrahydro-14H,29H-bis[1,2,4]triazolo[4,3-f:3,4-m]dibenzo[b,q][1,19]dioxa[8,12]dithia[5,6,14,15]tetraazacyclodocosine 
• 875769-91-8 2,2'-(2,2'-(propane-1,3-diylbis(oxy))bis(2,1-phenylene))bis(methylene)-bis(N-benzylbenzenamine) 
• 1122580-54-4 1,3-bis(o-{[3-Mercapto-5-pyridin-4-yl-[1,2,4]triazol-4-ylimino]-methyl}-phenoxy)-propane 
• 1122580-71-5 1,3-bis(2-{[5-Mercapto-[1,3,4]thiadiazol-2-ylimino]-methyl}-phenoxy)-propane 
• 1122580-55-5 1,3-bis{[[5-(pyridin-3-yl)-3-thioxo-2H-3,4-dihydro-[1,2,4]triazol-4-ylimino]methyl]phenoxy}propane 

Relevant academic research and scientific papers

Synthesis of new dihydroxy-dioxygenated ortho-[2,x]cyclophanes

The synthesis of title compounds (1a-f) by intramolecular reductive coupling is presented. The reaction is carried out in water solution, in the presence of Zn or Al powder, in basic media.

Synthesis and spectral studies of macrocyclic Cu(II), Ni(II) and Co(II) complexes by template reaction of 1,4-bis(3-aminopropoxy)butane with metal(II) nitrate and salicylaldehyde derivatives

Six new macrocyclic complexes were synthesized by template reaction of salicylaldehyde derivatives with 1,4-bis(3-aminopropoxy)butane and metal(II) nitrate. The metal to ligand ratio of the complexes was found to be 1:1. The Cu(II) complexes are proposed

Synthesis and characterization of new modified silica coated magnetite nanoparticles with bisaldehyde as selective adsorbents of Ag(i) from aqueous samples

In this study, new silica-coated magnetic nanoparticles modified with bisaldehyde (BISA-APTSCMNPs) were synthesized using a normal method and a vice versa method. The crystal structure of the newly obtained nanoparticles was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Vibrating Sample Magnetometry (VSM), thermogravimetric analysis (TGA) and ultra-violet visible spectroscopy (UV-vis). The surface of the nanoparticles was modified with bisaldehyde (BISA-APTSCMNPs), and these were used for the highly selective removal of Ag(i) ion from an aqueous mixed metal ion solution containing Cu(ii), Co(ii), Ni(ii), Zn(ii) and Pb(ii) using the syringe and batch techniques. Moreover, the silver ion desorption was most efficient in HCl.

Nanodimensional microreactors encapsulation of 15- and 16-membered diaza dioxa macrocyclic Schiff-base copper(II) complex nanoparticles: Synthesis and characterization

Copper(II) complexes with 15- and 16-membered diaza dioxa Schiff-base macrocyclic ligands "[Cu(R[15 or 16]N2O2)]2+ (R = Et, Pr, Ph, Ch)" were entrapped in the nanopores of zeolite-Y by a three-step process in the liquid ph

Synthesis, characterization and spectroscopy studying of some metal complexes of a new Schiff base ligand; X-ray crystal structure, NMR and IR investigation of a new dodecahedron Cd(II) complex

Some new [Cd(H2L1)(NO3)]ClO4 (1), [Mn(H2L1)](ClO4)2 (2), [Ni(H2L1)](ClO4)2 (3) and [Cu(H2L1)](ClOsub

Synthesis and biochemical activity studies of 2,2'-[propane-1,3- diylbis(oxy)]-2,2'bis-[(benzylideneamino)benzenethiol] ligand and its mononuclear Copper(II), Nickel(II), and Cobalt(II) complexes

A new hexadentate ligand incorporating Schiff base moities has been synthesized and its copper(II), nickel(II), and cobalt(II) complexes have been prepared and characterized by spectral methods. Elemental analyses and spectroscopic data of the Schiff base ligand and its copper(II), nickel(II), and cobalt(II) complexes are consistent with the formation of the ligand and its metal complexes. In addition to the Schiff base ligand (H2L) and copper (II), nickel(II), and cobalt(II) complexes (5-7) were tested against the morphology of series bacteria. The copper(II), nickel(II), and cobalt(II) complexes exhibit higher activity than Schiff base ligand (H2L) under identical experimental conditions. Copyright Taylor and Francis Group, LLC.

Design and synthesis of rhodamine based chemosensors for the detection of Fe3+ ions

The number and nature of coordinating entities as well as the size of chelating cavity in rhodamine based chemosensors were tuned to enhance the selectivity and sensitivity for Fe3+ ions. An intense pink color development and enhancement in flu

Pinacolophanes as versatile precursor for the practical synthesis of tolanophanes

Abstract: A new strategy for the synthesis of tolanophanes was investigated. The coupling of bridged dialdehydes gave selectively the corresponding monomer of pinacolophanes in quantitative yields under a simple and clean reaction condition. Without any f

Novel 2-cyanoacrylamido-4,5,6,7-tetrahydrobenzo[b]thiophene derivatives as potent anticancer agents

Ethyl 2-acrylamido-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate as well as its corresponding bis-derivatives, 5–10, with aliphatic linkers were synthesized, fully characterized, and tested as novel anticancer agents. The targeted compounds, 5–10, wer

Zeolite encapsulated Ni(ii) and Cu(ii) complexes with tetradentate N 2O2 Schiff base ligand: Catalytic activity towards oxidation of benzhydrol and degradation of rhodamine-B

Nickel(ii) and copper(ii) complexes of the Schiff base ligand O,O′-trimethyl bis (salicylidene isonicotinylhydrazone) (H2L) were synthesized and characterized. The encapsulation of these complexes in the cavities of the zeolite was achieved by