2403-53-4 Usage
Description
2-(4-nitrophenyl)-1,3-dioxolane, also known as 4-Nitrophenyl-1,3-dioxolane, is a cyclic organic compound belonging to the class of dioxolanes. It features a phenyl ring with a nitro group attached and contains two oxygen atoms and four carbon atoms. This colorless liquid possesses a sweet, floral odor and is recognized for its flammable nature and potential hazards, necessitating careful handling.
Uses
Used in Pharmaceutical Industry:
2-(4-nitrophenyl)-1,3-dioxolane is used as a solvent in the pharmaceutical industry for its ability to dissolve a wide range of compounds, facilitating the manufacturing and formulation of various drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-nitrophenyl)-1,3-dioxolane serves as a solvent, aiding in the production and application of agricultural chemicals to enhance crop protection and yield.
Used in Electronics Industry:
2-(4-nitrophenyl)-1,3-dioxolane is utilized as a solvent in the electronics industry, where it plays a role in the manufacturing processes of electronic components and devices, contributing to their functionality and performance.
Used as a Reagent in Organic Synthesis:
2-(4-nitrophenyl)-1,3-dioxolane is employed as a reagent in organic synthesis, enabling the formation of various complex organic molecules for use in different chemical and industrial applications.
Used as an Intermediate in Chemical Production:
2-(4-nitrophenyl)-1,3-dioxolane also functions as an intermediate in the production of other chemicals, highlighting its versatility and importance in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 2403-53-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2403-53:
(6*2)+(5*4)+(4*0)+(3*3)+(2*5)+(1*3)=54
54 % 10 = 4
So 2403-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c11-10(12)8-3-1-7(2-4-8)9-13-5-6-14-9/h1-4,9H,5-6H2
2403-53-4Relevant articles and documents
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Kobayashi et al.
, p. 1785 (1966)
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Danen,W.C. et al.
, p. 4830 - 4834 (1972)
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Application of poly(Vinylbenzyltrimethylammonium tribromide) resin as an efficient polymeric catalyst in the acetalization and diacetylation of benzaldehydes
Han, Bingbing,Hu, Junjun,Li, Xianwei,Zheng, Zubiao
supporting information, p. 287 - 293 (2021/04/28)
The applications of a new supported tribromide reagent (poly(vinylbenzyltrimethylammonium tribromide) resin) were reported. This supported tribromide resin was used as a catalyst in the acetalization and diacetylation of benzaldehydes under mild conditions with high efficiency. The effects of solvents, and amount of the supported tribromide resin on the reactions were investigated. Under the optimal conditions, most of acetal and 1,1-diacetates of benzaldehydes were selectively obtained in excellent yields.
Palladium-Catalyzed Mizoroki-Heck Reaction of Nitroarenes and Styrene Derivatives
Okita, Toshimasa,Asahara, Kitty K.,Muto, Kei,Yamaguchi, Junichiro
supporting information, p. 3205 - 3208 (2020/04/10)
We have developed a Mizoroki-Heck reaction of nitroarenes with alkenes under palladium catalysis. The use of a Pd/BrettPhos catalyst promoted the alkenylation, whereas other catalysts led to a decrease in the product yield. In addition to nitroarenes, nitroheteroarenes were also applicable to the present reaction. The combination of a nucleophilic aromatic substitution (SNAr) with the denitrative alkenylation produced a multifunctionalized arene in a one-pot operation.