60758-87-4

Usage

Uses

Used in Pharmaceutical Industry:
3,4-diethoxybenzonitrile is used as an intermediate in the production of pharmaceuticals for its ability to be synthesized into various medicinal compounds, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 3,4-diethoxybenzonitrile serves as an intermediate, playing a crucial role in the synthesis of agrochemicals that aid in crop protection and enhancement of agricultural yields.
Used in Dye and Pigment Manufacturing:
3,4-diethoxybenzonitrile is utilized as a precursor in the manufacturing of dyes and pigments, enabling the creation of a wide range of colorants for various applications.
Used in Organic Synthesis as a Solvent:
3,4-diethoxybenzonitrile acts as a solvent in organic synthesis, facilitating various chemical reactions due to its unique properties as a liquid at room temperature.
Used in Chemical Reactions as a Reagent:
3,4-diethoxybenzonitrile is employed as a reagent in chemical reactions, participating in the transformation of other compounds to achieve desired outcomes in chemical processes.
Safety and Handling:
It is important to handle 3,4-diethoxybenzonitrile with care, as it may cause irritation to the skin, eyes, and respiratory system upon exposure. To ensure safety, it should be kept in a tightly sealed container and stored in a cool, dry place away from heat and flame.

InChI:InChI=1/C11H13NO2/c1-3-13-10-6-5-9(8-12)7-11(10)14-4-2/h5-7H,3-4H2,1-2H3

Upstream product

• 81259-55-4 3,4-diethoxy-benzaldehyde-oxime 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 98-09-9 benzenesulfonyl chloride 
• 2029-94-9 3,4-diethoxybenzaldehyde 
• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 

Downstream Products

• 349446-71-5 3,4-diethoxy-benzoic acid amide 
• 60759-00-4 3,4-diethoxybenzthioamide 
• 1201448-00-1 C₁₁H₁₆N₂O₃ 
• 1201447-97-3 methyl 3,4-diethoxybenzimidate 
• 1201443-99-3 4-(5-(3,4-diethoxyphenyl)-4H-1,2,4-triazol-3-yl)pyridine 
• 878981-38-5 3-(3,4-diethoxyphenyl)-5-(pyridin-4-yl)-1,2,4-oxadiazole 
• 160322-96-3 4-[2-(3,4-Diethoxy-phenyl)-thiazol-4-yl]-benzoic acid methyl ester 
• 160322-91-8 methyl 6-<2-(3,4-diethoxyphenyl)thiazol-4-yl>pyridine-2-carboxylate 
• 160322-92-9 3-[2-(3,4-Diethoxy-phenyl)-thiazol-4-yl]-benzoic acid methyl ester 
• 145739-56-6 6-[2-(3,4-diethoxyphenyl)-thiazole-4-yl]pyridine-2-carboxylic acid 
• 160322-95-2 5-[2-(3,4-Diethoxy-phenyl)-thiazol-4-yl]-thiophene-2-carboxylic acid methyl ester 
• 160322-94-1 5-[2-(3,4-Diethoxy-phenyl)-thiazol-4-yl]-furan-2-carboxylic acid methyl ester 
• 160322-93-0 2-[2-(3,4-Diethoxy-phenyl)-thiazol-4-yl]-benzoic acid methyl ester 

Relevant academic research and scientific papers

Process for preparing 3,4-dihydroxy-benzonitrile

A process for preparing 3,4-dihydroxybenzonitrile includes the steps of reacting a nitrile compound with an alkali metal halide, followed by treating with an acid.

An efficient method for the preparation of nitriles via the dehydration of aldoximes with phthalic anhydride

A new and highly efficient method for the conversion of aldoximes to nitriles was established. By fusing with phthalic anhydride, aldoximes were efficiently and smoothly converted into nitriles, in high yields (over 85%) and in a short time (within 5 minutes). The mixture of phthalic anhydride, a cyclic anhydride, and aldoximes in fusing state set up an ideal transition state for a selective [3.3]-sigmatropic rearrangement of the acylated aldoximes to nitriles.

A new one pot method for the conversion of aldehydes into nitriles using hydroxyamine and phthalic anhydride

The aryl and alkyl aldehydes were readily converted to give the corresponding nitrites in good yields using hydroxyamine and phthalic anhydride as reagents in one pot.