43035-14-9

Usage

Uses

Used in Dye Industry:
Benzenamine, 3-ethoxy-N-phenyl(9CI) is used as an intermediate for the production of various dyes. It plays a crucial role in the synthesis of a wide range of dyes, contributing to the color and stability of the final products.
Used in Pharmaceutical Industry:
Benzenamine, 3-ethoxy-N-phenyl(9CI) is used as an intermediate in the manufacturing of pharmaceuticals. Its unique chemical properties make it a valuable component in the development of various medications.
Used in Rubber Chemical Industry:
Benzenamine, 3-ethoxy-N-phenyl(9CI) is used in the production of rubber chemicals. It helps improve the performance and durability of rubber products by enhancing their resistance to wear and tear.
Used in Antioxidant Production:
Benzenamine, 3-ethoxy-N-phenyl(9CI) is used in the production of antioxidants. These antioxidants are essential in preventing the degradation of materials and extending their shelf life, particularly in the plastics and rubber industries.
Safety Precautions:
Benzenamine, 3-ethoxy-N-phenyl(9CI) may cause skin and eye irritation upon contact. It should be handled with care in a well-ventilated area to minimize potential health risks.

Upstream product

• 64-67-5 diethyl sulfate 
• 101-18-8 3-hydroxy-N-phenylaniline 
• 75-03-6 ethyl iodide 
• 90555-66-1 (3-ethoxyphenyl)boronic acid 
• 62-53-3 aniline 
• 74-96-4 ethyl bromide 

Downstream Products

• 19950-91-5 4-ethoxy-N²-phenyl-o-phenylenediamine 
• 860576-86-9 N-(3-ethoxy-4-nitro-phenyl)-N-phenyl-acetamide 
• 859942-18-0 N-phenyl-N-(3-ethoxy-phenyl)-acetamide 
• 109690-33-7 2-ethoxy-N⁴-phenyl-p-phenylenediamine 

Relevant academic research and scientific papers

ALKYLATED ALKOXYDIARYLAMINE ANTIOXIDANTS

Alkylated diaryl amines further substituted by an alkoxy group on one or more aryl carbon atoms exhibit excellent antioxidant activity in lubricant compositions.

Copper-mediated N- and O-arylations with arylboronic acids in a continuous flow microreactor: a new avenue for efficient scalability

A continuous flow procedure has been elaborated for the copper(II)-mediated N- and O-arylation of a range of compounds with arylboronic acids using a commercial microreactor setup. The compounds could be continuously generated in good yields paving the way for efficient scalability.

Condensations of 1,4-Cyclohexanediones and Secondary Aromatic Amines. II. N-Phenylation of Diarylamines

The condensations of 1,4-cyclohexanedione with several diphenylamines were investigated in order to determine the limit of the utility of this reaction for the N-phenylation of aromatic secondary amines. 4-Methoxy-, 4,4'-dimethyl-, and 4,4'-dibromodiphenylamines produced their N-phenylated compounds in fairly good yields, but 4-hydroxy-, 3-methoxy-, and 4,4'-bis(dimethylamino)diphenylamines produced poor yields.Nitro-substituted diphenylamines gave N-phenyl derivatives in low yields along with N-4-hydroxyphenyl derivatives.N,N'-Diphenyl-p-phenylenediamine and N,N'-diphenylbenzidine gave correspondig tetra-N-phenyl diamines in good yields.The condensation of N-phenyl-1-naphthylamine, N-phenyl-2-naphthylamine, di-2-pyridylamine, phenothiazine, and carbazole with 1,4-cyclohexanedione were also examined.