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Usage

Uses

Used in Pharmaceutical Industry:
2-(4-Cyanophenyl)-1,3-dioxolane is used as a pharmaceutical intermediate for the synthesis of various drugs. Its chemical properties allow it to be a key component in the creation of new medicinal compounds, contributing to the development of novel treatments and therapies.
Used in Perfumery:
In the fragrance industry, 2-(4-Cyanophenyl)-1,3-dioxolane serves as a solvent in the production of perfumes. Its ability to dissolve a wide range of aromatic compounds makes it an essential ingredient in formulating complex and long-lasting scents.
Used in Organic Chemistry:
As a reagent in organic chemistry, 2-(4-Cyanophenyl)-1,3-dioxolane is utilized in various chemical reactions due to its capacity to participate in a range of organic transformations, facilitating the synthesis of diverse organic compounds.
Used in Metal Ion Complexation:
2-(4-Cyanophenyl)-1,3-dioxolane is used as a complexing agent for metal ions, forming stable and soluble complexes. This property is particularly valuable in the extraction and separation of metal ions from various solutions, playing a crucial role in analytical chemistry and metallurgical processes.
Used in Polymer Chemistry:
Due to its unique structure and reactivity, 2-(4-Cyanophenyl)-1,3-dioxolane has been studied for its potential applications in polymer chemistry. It is being explored for its ability to influence the properties of polymers, potentially leading to advancements in material science and the development of new polymeric materials with specific characteristics.

InChI:InChI=1/C10H9NO2/c11-7-8-1-3-9(4-2-8)10-12-5-6-13-10/h1-4,10H,5-6H2

Upstream product

• 107-21-1 ethylene glycol 
• 105-07-7 4-cyanobenzaldehyde 
• 623-00-7 4-bromobenzenecarbonitrile 
• 646-06-0 1,3-DIOXOLANE 
• 1663-39-4 tert-Butyl acrylate 
• 630-18-2 tert-butyl isocyanide 
• 10602-01-4 p-bromobenzaldehyde 1,3-dioxolane 
• 3058-39-7 4-iodobenzonitrile 
• 623-03-0 4-Cyanochlorobenzene 

Downstream Products

• 104566-44-1 4-(1,3-dioxacyclopent-2-yl)benzylamine 
• 444169-52-2 2-hydroxyethyl 4-cyanobenzoate 
• 636589-43-0 2-[(Z)-p-cyanobenzylidene]-3,3,5,5-tetramethylcyclohexanone 
• 636589-42-9 2,6-bis[(Z)-p-cyanobenzylidene]-3,3,5,5-tetramethylcyclohexanone 
• 875582-80-2 tert-butyl [4-(1,3-dioxolan-2-yl)benzyl]carbamate 
• 156866-52-3 tert-butyl N-(4-formylbenzyl)carbamate 
• 868280-61-9 1-[4-(1,3-dioxolan-2-yl)phenyl]-2-phenylethanone 
• 80463-23-6 4-(1,3-dioxolan-2-yl)acetophenone 
• 1240309-56-1 1-(4-(1,3-dioxolan-2-yl)phenyl)-2-(3-(trifluoromethyl)phenyl)ethanone 
• 1240309-67-4 1-(4-(1,3-dioxolan-2-yl)phenyl)hexan-1-one 
• 105-07-7 4-cyanobenzaldehyde 
• 1444001-60-8 4-(1,3-dioxolan-2-yl)-N'-((ethoxycarbonyl)oxy)benzimidamide 
• 1444001-53-9 (R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate 
• 1456890-20-2 N-(4-formylbenzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide 

Relevant academic research and scientific papers

A nitroolefin functionalized DPP fluorescent probe for the selective detection of hydrogen sulfide

In this paper, a nitroolefin functionalized probe DPP-NO2 was designed and synthesized as a selective fluorescent probe for detection of hydrogen sulfide (H2S). The specific reduction reaction between the nitro group and H2/sub

A Colorimetric and Fluorescent Probe Based on Michael Acceptor Type Diketopyrrolopyrrole for Cyanide Detection

A new probe 1 was synthesized by incorporating an α,β-unsaturated ketone to a diketopyrrolopyrrole fluorophore. The probe exhibited a selective and sensitive response to cyanide against other anions. Addition of CN? aqueous solution to 1 result

Porosity-induced emission: exploring color-controllable fluorescence of porous organic polymers and their chemical sensing applications

Most organic dyes dissipate their excitation energy in the aggregated state because of the "aggregation-caused quenching" effect, deteriorating their application in optoelectronic devices. To prevent the "aggregation-caused quenching" effect, we incorpora

Synthesis and remarkable mechano- and thermo-hypsochromic luminescence of a new type of DPP-based derivative

Owing to academic significance and potential applications, mechanofluorochromism has attracted much research interest. However, among the hundreds of mechanofluorochromic organic and metallorganic compounds reported to date, those with high contrast, mult

A colorimetric probe based on diketopyrrolopyrrole and tert-butyl cyanoacetate for cyanide detection

A new colorimetric probe 1 comprising a diketopyrrolopyrrole-based Michael receptor, which recognized cyanide anions with high selectivity, was designed and synthesized. Addition of CN- aqueous solution to 1 in THF resulted in a rapid color cha

A cyanide-selective colorimetric "naked-eye" and fluorescent chemosensor based on a diketopyrrolopyrrole-hydrazone conjugate and its use for the design of a molecular-scale logic device

A novel diketopyrrolopyrrole (DPP)-hydrazone based receptor 1 was designed and synthesized as a selective fluorescent and colorimetric chemosensor for cyanide without interference from other common anions including fluoride and acetate. The spectral respo

Photochemical C-H Activation Enables Nickel-Catalyzed Olefin Dicarbofunctionalization

Alkenes, ethers, and alcohols account for a significant percentage of bulk reagents available to the chemistry community. The petrochemical, pharmaceutical, and agrochemical industries each consume gigagrams of these materials as fuels and solvents each year. However, the utilization of such materials as building blocks for the construction of complex small molecules is limited by the necessity of prefunctionalization to achieve chemoselective reactivity. Herein, we report the implementation of efficient, sustainable, diaryl ketone hydrogen-atom transfer (HAT) catalysis to activate native C-H bonds for multicomponent dicarbofunctionalization of alkenes. The ability to forge new carbon-carbon bonds between reagents typically viewed as commodity solvents provides a new, more atom-economic outlook for organic synthesis. Through detailed experimental and computational investigation, the critical effect of hydrogen bonding on the reactivity of this transformation was uncovered.

Ammonium Chloride-Promoted Rapid Synthesis of Monosubstituted Ureas under Microwave Irradiation

Monosubstituted ureas are important scaffolds in organic chemistry. They appear in various biologically active compounds and serve as versatile precursors in synthesis. Monosubstituted ureas were originally prepared using toxic and hazardous phosgene equivalents. Modern methods include transamidation of urea and nucleophilic addition to cyanate salts, both of which suffer from a narrow substrate scope due to the need for a strong acid and prolonged reaction times. We hereby report that ammonium chloride can promote the reaction between amines and potassium cyanate to generate monosubstituted ureas in water. This method proceeds rapidly under microwave irradiation and tolerates a broad range of functional groups. Unlike previous strategies, it is compatible with other nucleophiles, acid-labile moieties, and most of the common protecting groups. The products precipitate out of solution, allowing facile isolation without column chromatography.

Ester compound based on pyrrolopyrrolediketone and having solid-liquid double fluorescence and application

The invention discloses an ester compound based on pyrrolopyrrolediketone and having solid-liquid double fluorescence, which has the following structural general formula; wherein the R1, R2, R3, R4 and R5 are respectively and independently selected from h

Beauty in chemistry: A self-organized and dual-phase emissive diketopyrrolopyrrole derivative as high-yield fluorescent material

In the long-span human history, “beauty” has always been the ultimate pursuit of mankind's civilization. In this work, we report the synthesis of a beautiful fluorescent material based on an old-brand pigment named diketopyrrolopyrrole (DPP) with a high y