77354-98-4

Usage

Uses

Used in Organic Chemistry:
2,2’-(1,4-Butanediyldioxy)bisbenzaldehyde is used as a building block for the synthesis of various organic compounds and materials. Its unique structure allows for the creation of new molecules with potential applications in different fields.
Used in Pharmaceutical Development:
2,2’-(1,4-Butanediyldioxy)bisbenzaldehyde is used as a starting material in the development of new pharmaceuticals. Its chemical properties and reactivity make it a promising candidate for the design and synthesis of novel drug molecules.
Used in Functional Materials:
2,2’-(1,4-Butanediyldioxy)bisbenzaldehyde is used in the development of functional materials. Its potential applications include the creation of new materials with specific properties, such as conductivity, magnetism, or catalytic activity, for use in various industries.

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 90-02-8 salicylaldehyde 
• 89-95-2 2-methyl-benzyl alcohol 
• 55-98-1 busulfan 
• 110-56-5 1,4-dichlorobutane 
• 4724-56-5 1,4-ditosyloxybutane 

Downstream Products

• 113038-69-0 2,2'-butanediyldioxy-di-benzaldehyde bis-carbamimidoylhydrazone 
• 134777-69-8 C₂₆H₂₈N₆O₈ 
• 389600-94-6 C₁₈H₂₀N₂O₄ 
• 122336-37-2 O,O'-Tetramethylenebis(salicylideneaniline) 
• 105068-22-2 O,O'-Tetramethylenebis(salicylidenebenzylamine) 
• 1165762-14-0 4-(2-(4-(2-(6-(3-nitrophenyl)-4-phenyl-1,3-diazabicyclo[3.1.0]hex-3-en-2-yl)phenoxy)butoxy)phenyl)-6-(3-nitrophenyl)-2-phenyl-3,5-diazabicyclo[3.1.0]hex-2-ene 
• 1257429-38-1 1,4-bis{[[5-(pyridin-3-yl)-3-thioxo-2H-3,4-dihydro-[1,2,4]triazol-4-ylimino]methyl]phenoxy}butane 
• 1421161-65-0 (N,N',N,N')-N,N'-(2,2'-(butane-1,4-diylbis(oxy))bis(2,1-phenylene))bis(methan-1-yl-1-ylidene)bis(3,5-diethyl-4H-1,2,4-triazol-4-amine) 
• 1421161-69-4 C₃₀H₄₂N₈O₂ 
• 1629992-67-1 C₂₄H₂₆O₄ 
• 166387-03-7 C₁₈H₂₀Cl₂O₂ 
• 1429339-59-2 1,4-bis(2-((allyloxy)methyl)phenoxy)butane 

Relevant academic research and scientific papers

Synthesis and structural characterization of new N2O2-donor Schiff base macrocycles and their silver(I) coordination polymers

Two N2O2-donor macrocyclic Schiff bases mD1 and mD2 (mD1 = 1,5-diaza-2,4:7,8:16,17-tribenzo-9,15-dioxa-cyclooctadeca-1,5-dien; mD2 = 1,5-diaza-2,4:7,8:15,16-tribenzo-9,14-dioxa-cycloheptadeca-1,5-dien) were prepared by the [1+1] cycl

[1+1] Copper(II) macrocyclic Schiff base complex on rGO as a photocatalyst for reduction of nitroaromatics compounds under visible-light irradiation

In this work, [1 + 1] macrocyclic Copper(II) Schiff base complex ([CuL](NO3)2.H2O) was synthesized and grafted on reduced graphene oxide successfully. The novel prepared sample was characterized by physico-chemical techniques and used as a photocatalyst for the reduction of nitroaromatic compounds to their amine derivatives at room temperature under visible-light irradiation with hydrazine mono hydrate. From the prepared samples, reduced graphene oxide loaded with 30% [CuL](NO3)2.H2O catalyst (rGO/CuM30) shows the best efficiency for converting different nitroaromatic compounds to the corresponding amino compounds using visible light. As-prepared catalyst illustrated excellent activity for the reduction of 2-nitrophenol to 2-aminophenol (100% conversion) in only 90 min. Finally, the catalyst could be recovered for five times and reused without decreasing of its efficiency.

Introduction of a trinuclear manganese(iii) catalyst on the surface of magnetic cellulose as an eco-benign, efficient and reusable novel heterogeneous catalyst for the multi-component synthesis of new derivatives of xanthene

In this work, the new trinuclear manganese catalyst defined as Fe3O4@NFC@NNSM-Mn(iii) was successfully manufactured and fully characterized by different techniques, including FT-IR, XRD, TEM, SEM, EDX, VSM, and ICP analysis. There have been reports of the use of magnetic catalysts for the synthesis of xanthine derivatives. The critical potential interest in the present method include short reaction time, high yields, recyclability of the catalyst, easy workup, and the ability to sustain a variety of functional groups, which give economical as well as ecological rewards. Also, the synthesized catalyst was used as a recyclable trinuclear catalyst in alcohol oxidation reactions at 40 °C. The magnetic catalyst activity of Fe3O4@NFC@NNSM-Mn(iii) could be attributed to the synergistic effects of the catalyst Fe3O4@NFC@NNS-Mn(iii) with melamine. Employing a sustainable and safe low temperature, using an eco-friendly solvent, no need to use any additive, and long-term stability and magnetic recyclability of the catalyst for at least six successive runs are the advantages of the current protocol towards green chemistry. This protocol is a benign, environmentally friendly method for heterocycle synthesis. This journal is

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

Prospective new amidinothiazoles as leukotriene B4 inhibitors

An efficient and one-step synthesis of the versatile, hitherto new derivatives resembling LY293111, a prospective potent antagonist of the leukotriene B4 (LTB4) receptor, were reported. The strategy was based on the synthesis of an amidinothiazole ring, c

Design, two-directional synthesis, DFT study of new pyrimido[5,4-d]pyrimidine-2,8-dione derivatives

A facile two-directional synthesis of new pyrimido[5,4-d]pyrimidine-2,8-dione was reported via an efficient reaction of premade bis-aldehydes and 1-(2-amino-1,2-dicyanovinyl)-3-phenylurea in the presence of triethylamine as the base and Cu (II) as catalys

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

Excellent alkene epoxidation catalytic activity of macrocyclic-based complex of dioxo-Mo(VI) on supermagnetic separable nanocatalyst

A phenoxybutane-based Schiff base complex of cis-dioxo-Mo(VI) was supported on paramagnetic nanoparticles and characterized using powder X-ray diffraction, infrared, diffuse reflectance and atomic absorption spectroscopies, scanning and transmission elect

Design and synthesis of a new class of 2,4-thiazolidinedione based macrocycles suitable for Fe3+ sensing

A new class of three 2,4-thiazolidinedione based macrocycles (3a-c) have been synthesized and then characterized from spectral data and X-ray crystallography. The fluorescence quenching of the compounds caused by the addition of nineteen separate metal cations to their solutions in ethanol-water (3 : 1) was investigated, when it was observed that among the cations, the response to Fe3+ was distinctive. Again, among the macrocycles, 3c gave the best result.

Facile one-pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers under mild conditions

We report here the facile, room temperature, catalyst free, one pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers. Anhydrous potassium carbonate (K2CO3) as a mild base along with dimethyl sulfoxide gener