59235-35-7

Basic information

• Product Name: ethyl 2-(4-aminophenyl)acetate
• Synonyms: ethyl 2-(4-aMinophenyl)acetate hydrochloride
• CAS NO: 59235-35-7
• Molecular Formula: C₁₀H₁₃NO₂*ClH
• Molecular Weight: 0
• Mol File: 59235-35-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: ethyl 2-(4-aminophenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(4-aminophenyl)acetate(59235-35-7)
• EPA Substance Registry System: ethyl 2-(4-aminophenyl)acetate(59235-35-7)

Safety Data

• Hazardous Substances Data: 59235-35-7(Hazardous Substances Data)

Usage

General Description

Ethyl 2-(4-aminophenyl)acetate is a chemical compound with the molecular formula C10H13NO2. It is an ester derived from acetic acid and 4-aminophenol, and it consists of an ethyl group attached to a 2-(4-aminophenyl)acetate group. ethyl 2-(4-aminophenyl)acetate is used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, including those with analgesic and anti-inflammatory properties. Ethyl 2-(4-aminophenyl)acetate is also utilized in the production of pigments, dyes, and other organic compounds, making it a versatile chemical with multiple applications in different industries. It is important to handle this compound with care, as it can be hazardous if not used properly.

Upstream product

• 64-17-5 ethanol 
• 1197-55-3 4-aminophenylacetic acid 
• 5445-26-1 ETHYL 4-NITROPHENYLACETATE 

Downstream Products

• 774602-80-1 {4-[2-(2-chloroethoxy)-acetylamino]-phenyl}-acetic acid ethyl ester 
• 169186-00-9 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-(tetrahydropyran-2-yloxy)butanamide 
• 169186-11-2 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)hexanamide 
• 169186-03-2 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-phenylbutanamide 
• 169186-07-6 (RS)-2-(4-bromobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-phenylbutanamide 
• 169186-10-1 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)pentanamide 
• 169186-13-4 (R)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)hexanamide 
• 169186-15-6 (RS)-2-(4-bromobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)hexanamide 
• 169186-19-0 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)octanamide 
• 169186-22-5 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-methylthiobutanamide 
• 169186-31-6 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-ethylthiobutanamide 
• 169186-36-1 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-3-phenylpropanamide 
• 169186-40-7 (RS)-2-(4-bromobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-3-phenylpropanamide 
• 169186-20-3 (RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-3-methylbutanamide 

Relevant articles and documents

Organosilicon synthesis of isocyanates: III. Synthesis of aliphatic, carbocyclic, aromatic, and alkylaromatic isocyanatocatboxylic acid esters

A series of aminoacid esters was prepared by treating the aminoacid suspensions in ethanol with thionyl chloride. Best conversion of aminoacid esters to corresponding isocyanates was achieved in the case of aromatic and carbocyclic aminoesters by phosgeneation of their N-silyl derivatives, and in the case of aliphatic and alkylaromatic aminoesters by phosgeneation of O-silyl or N,O-bissilylurethanes on their basis. In the last case additional step of esterification of the by-products isocyanatoalkylcarboxylic acid chlorides is required after phosgeneation. Unusual generation of cynnamates and intramolecular N→O-migration of trimethylsilyl group in the solutions of silylated alkylaromatic β-aminoacid esters were found. Pleiades Publishing, Inc., 2006.