17954-12-0

Basic information

• Product Name: 2,2’-(1,3-Propanediyldioxy)bisbenzaldehyde
• Synonyms: 2,2’-(1,3-Propanediyldioxy)bisbenzaldehyde;-(1,3-Propanediyldioxy)bisbenzaldehyde;2,2’2,2'-(1,3-propanediyldioxy) bisbenzalde
• CAS NO: 17954-12-0
• Molecular Formula: C₁₇H₁₆O₄
• Molecular Weight: 284.309
• Mol File: 17954-12-0.mol
• Article Data: 33

Chemical Properties

• Melting Point: 97-98 °C
• Boiling Point: 467.1±25.0 °C(Predicted)
• Appearance: /
• Density: 1.193±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2,2’-(1,3-Propanediyldioxy)bisbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2’-(1,3-Propanediyldioxy)bisbenzaldehyde(17954-12-0)
• EPA Substance Registry System: 2,2’-(1,3-Propanediyldioxy)bisbenzaldehyde(17954-12-0)

Safety Data

• Hazardous Substances Data: 17954-12-0(Hazardous Substances Data)

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

Downstream Products

• 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 
• 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 
• 134777-68-7 C₂₅H₂₆N₆O₈ 
• 158629-86-8 2-[Hydroxy-(2-{3-[2-(1-hydroxy-2-methoxycarbonyl-allyl)-phenoxy]-propoxy}-phenyl)-methyl]-acrylic acid methyl ester 
• 141070-37-3 C₅₁H₄₈Cl₈N₄O₂ 

Relevant articles and documents

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 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.

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

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

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

A comparative molecular structure – NLO activity study of ortho-bridged dibenzaldehydes: Synthesis, crystal structure, SHG, and DFT studies

Structural and second order nonlinear optical characteristics of four ortho-bridged dibenzaldehydes with alkyloxy- and xylenyloxy linkers are compared from the XRD, UV-Vis-NIR spectroscopic, SHG, and DFT studies. Interruption of electron polarization by π

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