4-Methoxyphenylacetamide

4-Methoxyphenylacetamide Suppliers list
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com
Company Name: Shandong Xiya Chemical Co., Ltd  
Tel: 13355009207 13355009207
Email: 3007715519@qq.com
4-Methoxyphenylacetamide Basic information
Product Name:4-Methoxyphenylacetamide
Synonyms:Benzeneacetamide, 4-methoxy-;2-(4-METHOXY-PHENYL)-ACETAMIDE;PARA METHOXYL PHENYL ACETAMIDE;PARA METHOXYPHENYL ACETAMIDE;P-METHOXYPHENYLACETAMIDE;4-Methoxybenzeneacetamide;Einecs 228-745-9;2-hydroxybenzoic acid [(1R,3R,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] ester
CAS:6343-93-7
MF:C9H11NO2
MW:165.19
EINECS:228-745-9
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
Mol File:6343-93-7.mol
4-Methoxyphenylacetamide Structure
4-Methoxyphenylacetamide Chemical Properties
Melting point 182-184°C
Boiling point 354.7±25.0 °C(Predicted)
density 1.123±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka16.37±0.40(Predicted)
color White to Off-White
BRN 2088040
CAS DataBase Reference6343-93-7(CAS DataBase Reference)
Safety Information
Safety Statements 22-24/25
HS Code 2924297099
MSDS Information
ProviderLanguage
ALFA English
4-Methoxyphenylacetamide Usage And Synthesis
Uses4-Methoxyphenylacetamide is a useful reagent in the preparation of novel pyrrolidone-based derivatives as potential p53-MDM2 inhibitors for use as potential antitumor agents.
Synthesis
4-Methoxybenzyl cyanide

104-47-2

4-METHOXYPHENYLACETAMIDE

6343-93-7

General procedure for the synthesis of 4-methoxybenzeneacetamide from p-methoxybenzeneacetonitrile: Ni NPs/HT catalyst (0.05 g) was added to a thick-walled pressure tube, followed by water (4 ml) and p-methoxybenzeneacetonitrile (1 mmol). The reaction mixture was placed in an oil bath at 120 °C and stirred vigorously. The reaction process was monitored by TLC analysis. Upon completion of the reaction, the reaction mixture was extracted with ethyl acetate and subsequently filtered to remove the catalyst. The filtrate was cooled to 0 °C to allow white crystals to precipitate. The crystalline product was collected by simple filtration and dried under vacuum at room temperature to give analytically pure 4-methoxyphenylacetamide. If the product did not precipitate, the reaction mixture was extracted with ethyl acetate followed by purification by silica gel column chromatography to finally obtain 4-methoxyphenylacetamide.

References[1] Synthesis, 1989, # 12, p. 949 - 951
[2] RSC Advances, 2015, vol. 5, # 9, p. 6365 - 6371
[3] Zeitschrift fur Chemie, 1980, vol. 20, # 10, p. 380 - 380
[4] Catalysis Communications, 2012, vol. 29, p. 109 - 113
[5] Green Chemistry, 2014, vol. 16, # 4, p. 2136 - 2141
4-Methoxyphenylacetamide Preparation Products And Raw materials
Raw materials4-Methoxybenzyl cyanide-->4-Methoxyphenylacetic acid
Preparation Products(4-Methoxy-3-nitrophenyl)acetic acid-->Methyl 4-methoxyphenylacetate
Tag:4-Methoxyphenylacetamide(6343-93-7) Related Product Information
oxyphenisatine di(acetate) S(-)-ATENOLOL Atenolol Bufexamac 3-(N,N-Diacetoxyethyl)amino-4-methoxyacetanilide 3'-Amino-4'-methoxyacetanilide 4-Acetylamino-2-(diallylamino)anisole N-[3-[(2-Cyanoethyl)amino]-4-methoxyphenyl]acetamide N-[3-[(2-Cyanoethyl)ethylamino]-4-methoxyphenyl]acetamide 4'-(Difluoromethoxy)acetanilide 4-Acetylamino-2-(bis(2-hydroxyethyl)amino)anisole 4-Acetylamino-2-(diethylamino)anisole (+)-4-[2-Hydroxy-3-[(1-methylethyl)-amino]propoxy]benzeneacetamide 2',5'-Dimethoxyacetanilide Ethyl 3-hydroxy-4,6-dimethoxy-2-oxoindoline-3-carboxylate (4-Butoxyphenyl)acetamide 3,4-Dimethoxyphenylacetic acid hydrazide 2-[4-(2,3-Epoxypropoxy)phenyl]acetamide