50651-39-3

Basic information

• Product Name: N-(4-METHOXY-3-NITROPHENYL)ACETAMIDE
• Synonyms: N-(4-METHOXY-3-NITROPHENYL)ACETAMIDE;4-methoxy-3-nitroacetaniline;n-(4-methoxy-3-nitrophenyl)-acetamid;4-METHOXY-3-NITROACETANILIDE;1-ACETYLAMINO-4-METHOXY-3-NITROBENZENE;4-methoxyl-3-nitroacetaniline;4-Methoxy-3-nitroacetailide;4'-Methoxy-3'-nitroacetanilde
• CAS NO: 50651-39-3
• Molecular Formula: C₉H₁₀N₂O₄
• Molecular Weight: 210.19
• EINECS: 256-686-9
• Product Categories: Intermediates of Dyes and Pigments;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 50651-39-3.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 424.1°C at 760 mmHg
• Flash Point: 210.3°C
• Appearance: /
• Density: 1.327g/cm³
• Vapor Pressure: 2.12E-07mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: N-(4-METHOXY-3-NITROPHENYL)ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-METHOXY-3-NITROPHENYL)ACETAMIDE(50651-39-3)
• EPA Substance Registry System: N-(4-METHOXY-3-NITROPHENYL)ACETAMIDE(50651-39-3)

Safety Data

• Hazardous Substances Data: 50651-39-3(Hazardous Substances Data)

Usage

General Description

N-(4-Methoxy-3-nitrophenyl)acetamide is a chemical compound with the molecular formula C10H10N2O4. It is an amide derivative of 4-methoxy-3-nitroaniline and is used in the synthesis of pharmaceuticals and organic compounds. This chemical is commonly used as an intermediate in the production of various drugs and is also used as a dye intermediate. It has also been studied for its potential biological and pharmacological properties, including its antibacterial and antifungal activities. Overall, N-(4-Methoxy-3-nitrophenyl)acetamide is a versatile chemical compound with various applications in the pharmaceutical and chemical industries.

InChI:InChI=1/C9H10N2O4/c1-6(12)10-7-3-4-9(15-2)8(5-7)11(13)14/h3-5H,1-2H3,(H,10,12)

Upstream product

• 51-66-1 4-methoxyacetanilide 
• 104-94-9 4-methoxy-aniline 
• 119-27-7 2,4-dinitroanisole 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 100-00-5 4-chlorobenzonitrile 
• 100-17-4 para-methoxynitrobenzene 
• 108-24-7 acetic anhydride 
• 7664-93-9 sulfuric acid 
• 7697-37-2 nitric acid 
• 577-72-0 4-methoxy-3-nitroaniline 

Downstream Products

• 6375-47-9 3-amino-4-methoxyacetanilide 
• 577-72-0 4-methoxy-3-nitroaniline 
• 257932-05-1 N-(4-methoxy-2,5-dinitrophenyl)acetamide 
• 118509-98-1 (E)-methyl 3-(4-methoxy-3-nitrophenyl)acrylate 
• 19433-93-3 3-acetylamino-6-methoxy-N,N-diethylaniline 
• 4513-20-6 3-N,N-diethylamino-4-methoxy-aniline 

Relevant articles and documents

Synthesis method of high-purity 2 - nitro -4-aminoanisole

The invention discloses a synthesis method of high-purity 2 -nitro -4-aminoanisole, wherein 2 - nitro -4-n-aminoanisole is synthesized through an assembly line. The assembly line comprises a reaction device, a discharging device and a cleaning device. The method comprises the following steps: A, feeding reaction raw materials into a reaction device for reaction. B, Use clear bottom device to carry out the stirring to phase transfer catalyst and reaction raw materials. C, Use the cleaning device to clean the bottom of reation kettle. D, The extrusion device is used to clean and blow the cleaning device and the bottom cleaning device, and the catalyst and the reaction raw material are pushed up and down. E: The extraction bucket is used to extract the product in the reaction liquid and the extracted reaction is continued to return to the reaction kettle. F, Use the discharging device to make the reaction all discharge. G, Wash the reaction liquid with the cleaning device, obtain the finished product.

Industrial production method for 2-amino-4-acetamidoanisole

The invention discloses an industrial production method for 2-amino-4-acetamidoanisole. The industrial production method comprises the following steps: (1) allowing paranitroanisole and hydrogen to undergo a catalytic hydrogenation reduction reaction in the presence of a catalyst A so as to obtain p-aminoanisole; (2) allowing the p-aminoanisole to undergo an acetylation reaction so as to obtain p-acetamidoanisole; (3) allowing the p-acetamidoanisole to undergo a nitration reaction so as to obtain 2-nitro-4-acetamidoanisole; and (4) allowing 2-nitro-4-acetamidoanisole and hydrogen to undergo two catalytic hydrogenation reduction reactions in the presence of a catalyst B so as to obtain the 2-amino-4-acetamidoanisole. The production method provided by the invention has the characteristics oflow production cost, high reaction selectivity, simple separation process, high product purity, no three wastes in the process of production, recyclability and continuous large-scale industrial production, and solves the disadvantages of high separation cost, low product purity, and large discharge amount and difficult treatment of three wastes in the prior art.

2 - Amino - 4 - acetamido anisole novel synthesis process (by machine translation)

The present invention provides a novel 2 - amino - 4 - acetamido anisole synthesis process, the usage of palladium bi-metal catalysts and the palladium/carbon catalyst to replace Rany - Ni catalyst, to the anisole on the nitro-selective catalytic hydrogenation, which not only reduces use Rany - Ni catalyst of post-industrial risks, while at the same time, the resulting 2 - amino - 4 - acetyl anisole purity higher, greater yield. (by machine translation)