6317-89-1

Basic information

• Product Name: 3-acetaMidophenyl acetate
• Synonyms: 3-acetaMidophenyl acetate;3-(acetylamino)phenyl acetate
• CAS NO: 6317-89-1
• Molecular Formula: C₁₀H₁₁NO₃
• Molecular Weight: 193.19924
• Mol File: 6317-89-1.mol
• Article Data: 22

Chemical Properties

• Melting Point: 99.5-100.5 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 377.2°Cat760mmHg
• Flash Point: 181.9°C
• Appearance: /
• Density: 1.206g/cm³
• Vapor Pressure: 6.86E-06mmHg at 25°C
• Refractive Index: 1.561
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• PKA: 14.58±0.70(Predicted)
• CAS DataBase Reference: 3-acetaMidophenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-acetaMidophenyl acetate(6317-89-1)
• EPA Substance Registry System: 3-acetaMidophenyl acetate(6317-89-1)

Safety Data

• Hazardous Substances Data: 6317-89-1(Hazardous Substances Data)

Usage

Uses

3''-Acetoxyacetanilide can be used as waste plant extract.

InChI:InChI=1/C10H11NO3/c1-7(12)11-9-4-3-5-10(6-9)14-8(2)13/h3-6H,1-2H3,(H,11,12)

Upstream product

• 108-24-7 acetic anhydride 
• 591-27-5 m-Hydroxyaniline 
• 621-42-1 meta-hydroxyacetanilide 
• 75-36-5 acetyl chloride 
• 30074-98-7 1-Acetyl-4(1H)-pyridinon 
• 108-46-3 recorcinol 
• 1189746-71-1 cyclohexane-1,3-dione monoxime 
• 554-84-7 meta-nitrophenol 

Downstream Products

• 712-34-5 3-hydroxy-4-nitroacetanilide 
• 67915-26-8 N-(5-hydroxy-2-nitrophenyl)acetamide 
• 90946-96-6 1-acetoxy-5-acetylamino-2,4-dinitro-benzene 
• 89102-03-4 3-acetoxy-4-nitroacetanilide 
• 40547-58-8 N-(4-acetyl-3-hydroxyphenyl)acetamide 
• 621-42-1 meta-hydroxyacetanilide 
• 116911-48-9 5-acetoxy-2-nitroacetanilide 
• 89102-04-5 3-(benzyloxy)-4-nitroacetanilide 
• 89102-05-6 N-(2-propenyl)-N-<3-(benzyloxy)-4-nitrophenyl>acetamide 
• 116911-49-0 4-amino-3-(benzyloxy)-N-(2-propenyl)acetanilide 
• 116911-50-3 N-Allyl-N-{3-benzyloxy-4-[N'-prop-(E)-ylidene-hydrazino]-phenyl}-acetamide 
• 60207-18-3 4'-amino-2'-methoxylacetophenone 
• 51410-08-3 N-(4-acetyl-3-methoxyphenyl)acetamide 
• 2476-29-1 4-amino-2-hydroxy-acetophenone 

Relevant articles and documents

Method for promoting acylation of amine or alcohol by carbon dioxide

The invention relates to a method for promoting acylation of amine or alcohol by carbon dioxide, which comprises the following steps of: mixing an amine compound, carboxylate or thiocarboxylate compound and a reaction solvent under the action of carbon dioxide, and reacting to obtain an amide compound, or under the action of carbon dioxide, mixing the alcohol compound, the thiocarboxylate compound and the reaction solvent [gamma]-valerolactone, and reacting to obtain the ester compound. According to the invention, under the promotion action of carbon dioxide, carboxylate or thiocarboxylate is used as an acylation reagent, and amine and alcohol are converted into amide and ester compounds in the absence of a transition metal catalyst, so that acylation reagents such as acyl chloride or anhydride with irritation and corrosivity are avoided; and the method has the advantages of simple operation, mild reaction conditions, high tolerance of substrate functional groups, strong applicability and high yield, and provides an efficient, reliable and economical preparation method for synthesis of amide and ester compounds.

Biogenic CuFe2O4 magnetic nanoparticles as a green, reusable and excellent nanocatalyst for acetylation reactions under solvent-free conditions

A convenient green method has been developed for the synthesis of biogenic CuFe2O4 magnetic nanoparticles using tea extracts within a very short reaction time. The prepared nanoparticles with an average size of 8.78 nm have been used as an effective catalyst for the acetylation of various alcohols, phenols and amines in good to excellent yields under solvent-free conditions. The catalyst was characterized by XRD, XPS, VSM, SEM and TEM study. A magnetic study of the fresh and recycled catalyst after the fourth cycle was performed by VSM measurement. The main advantages of this protocol are simple biogenic synthesis of the catalyst, a reusable and heterogeneous catalytic system, and short reaction times with excellent yields.

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