43035-14-9

Basic information

• Product Name: Benzenamine, 3-ethoxy-N-phenyl- (9CI)
• Synonyms: Benzenamine, 3-ethoxy-N-phenyl- (9CI);3-Ethoxydiphenylamine
• CAS NO: 43035-14-9
• Molecular Formula: C₁₄H₁₅NO
• Molecular Weight: 213.275
• Product Categories: ETHOXY
• Mol File: 43035-14-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 343.9 °C at 760 mmHg
• Flash Point: 139.9 °C
• Appearance: /
• Density: 1.088 g/cm³
• CAS DataBase Reference: Benzenamine, 3-ethoxy-N-phenyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3-ethoxy-N-phenyl- (9CI)(43035-14-9)
• EPA Substance Registry System: Benzenamine, 3-ethoxy-N-phenyl- (9CI)(43035-14-9)

Safety Data

• Hazardous Substances Data: 43035-14-9(Hazardous Substances Data)

Usage

General Description

Benzenamine, 3-ethoxy-N-phenyl- (9CI), also known as 3-ethoxyaniline, is an organic compound with the chemical formula C8H11NO. It is a clear to slightly yellow liquid with a faint amine odor. This chemical is commonly used as an intermediate in the manufacturing of various dyes and pharmaceuticals. It is also used in the production of rubber chemicals, antioxidants, and other organic compounds. Benzenamine, 3-ethoxy-N-phenyl- (9CI) may cause skin and eye irritation upon contact and should be handled with care in a well-ventilated area.

Upstream product

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

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 articles and documents

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.

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.