2983-74-6

Usage

Uses

Used in Pharmaceutical Industry:
Cyanic acid, 4-methoxyphenyl ester is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its role in this industry is crucial for the development of new drugs, given its reactivity and ability to form key structural components within medicinal compounds.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, this ester functions as an intermediate in the synthesis of agrochemicals. It contributes to the creation of substances that are vital for crop protection and enhancement of agricultural productivity.
Safety Considerations:
Given its toxic nature, cyanic acid, 4-methoxyphenyl ester requires careful handling to prevent irritation to the skin, eyes, and respiratory system. It is imperative to adhere to proper safety protocols in laboratory and industrial environments to mitigate any potential hazards associated with its use.

Upstream product

• 506-68-3 bromocyane 
• 1122-93-6 potassium p-methoxyphenolate 
• 506-77-4 cyanogen chloride 
• 150-76-5 4-methoxy-phenol 
• 940-58-9 4-methoxyphenyl chlorothionoformate 

Downstream Products

• 651306-29-5 C₈H₁₀N₂O₃ 
• 6488-78-4 5-(4-methoxyphenoxy)tetrazole 
• 10381-16-5 O-4-methoxyphenyl thiocarbamate 
• 1352031-52-7 5-(4-methoxyphenoxy)-1,2,4-dithiazole-3-one 
• 52805-57-9 N,N-Diethyl-O-(4-methoxyphenyl)-N'-(phenylcarbamoyl)-isoharnstoff 
• 63082-07-5 4-methoxy-phenylcarbamate 
• 18218-51-4 N-tert.-Butyl-carbamidsaeure-(p-methoxy-phenylester) 
• 40588-09-8 Kohlensaeure-methylester-p-anisylesterimid 
• 25940-64-1 2,4,6-tris(4-methoxyphenoxy)-1,3,5-triazine 
• 74383-46-3 2-<(4-Methoxy)phenoxy>-3,4,5,6-tetraphenyl-pyridin 
• 111659-22-4 N-[3-(4-Methoxy-phenoxy)-[1,2,4]thiadiazol-5-yl]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine 

Relevant academic research and scientific papers

Synthesis and structure of substituted 5-phenoxy-1,2,4-dithiazole-3-ones

Seven new substituted 5-phenoxy-1,2,4-dithiazole-3-ones were prepared in modest yield (53-76%) from corresponding O-phenyl thiocarbamates and chlorocarbonylsulfenyl chloride in dry ether at-10 °C. All of the compounds were characterized by NMR and elemental analysis and some of them by X-ray diffraction. Preliminary kinetic measurements showed that the parent 5-phenoxy-1,2,4-dithiazole-3-one is a very efficient sulfurizing agent toward triphenyl phosphite. Copyright

Interaction of aryloxychlorocarbenes with acetylenedicarboxylate: Novel formation of polyfunctional butadienes and 8-oxatricyclo[3.2.1.0 2.4]oct-6-enes

The interaction of aryloxychlorocarbenes with dialkyl acetylenedicarboxylates has been examined. Thermolyses of 3-aryloxy-3- chlorodiazirines in the presence of acetylenedicarboxylate resulted in the formation of unexpected polyfunctional 1,3-butadienes and 8-oxatricyclo[3.2.1. 02.4]oct-6-enes or of 2-aryoxycarbonylmaleates dependent upon reaction conditions. This work confirmed the nucleophilicity of aryloxychlorocarbenes and underlined their synthetic potential.

Quantitative gas-solid reactions with ClCN and BrCN: Synthesis of cyanamides, cyanates, thiocyanates, and their derivatives

Gas-solid reaction techniques allow quantitative cyanations with ClCN and BrCN. Three primary and four secondary cyanamides, a cyanimide, four cyanates, and four thiocyanates were all prepared as solids in 100% yield from solid anilines, benzimidazoles, imides, phenolates, and thiolates, respectively. Intramolecular solid-state reactions of cyanated o-aminophenol and of cyanated hydrazides gave heterocyclic compounds. When comparable reactions were performed in solution the reported product yields were considerably less than 100% in all cases. The reasons for the success of the environmentally benign solid-state syntheses are discussed in terms of phase rebuilding, phase transformation, and crystal disintegration. Atomic force microscopy (AFM) of selected systems indicates the occurrence of long-range molecular movements which are governed by the crystal packing. This is evident from the obvious correlations between the molecular movements and the known crystal packing data. A new type of geometric surface feature, a rectangular and a rhombic depression which resembles a swimming-pool basin, was found in the cyanation of o-aminophenol and benzohydrazide.