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

Downstream Products

• 1370443-62-1 C₁₆H₁₅NO₄ 
• 1370443-61-0 C₁₆H₁₅NO₃S 
• 1146925-40-7 C₁₉H₁₉NO₄ 
• 1092298-41-3 7-amino-2-(4-ethoxyphenyl)-4H-chromen-4-one 
• 1370443-60-9 (E)-1-(4-amino-2-hydroxyphenyl)-3-(5-methylfuran-2-yl)prop-2-en-1-one 
• 1370443-59-6 (E)-1-(4-amino-2-hydroxyphenyl)-3-(5-methylthiophen-2-yl)prop-2-en-1-one 
• 1370443-58-5 (E)-1-(4-amino-2-hydroxyphenyl)-3-(4-ethoxyphenyl)prop-2-en-1-one 
• 1448348-99-9 (E)-1-(4-amino-2-hydroxyphenyl)-3-(4-(methylthio)phenyl)prop-2-en-1-one 
• 1448349-00-5 (E)-1-(4-amino-2-hydroxyphenyl)-3-(3-methoxyphenyl)-prop-2-en-1-one 
• 1448349-01-6 (E)-1-(4-amino-2-hydroxyphenyl)-3-(4-fluorophenyl)prop-2-en-1-one 
• 1448349-02-7 (E)-1-(4-amino-2-hydroxyphenyl)-3-(4-chlorophenyl)prop-2-en-1-one 
• 1448349-03-8 (E )-1-(4-amino-2-hydroxyphenyl)-3-(3,5-bis-(trifluoromethyl)phenyl)prop-2-en-1-one 
• 1448349-04-9 (E)-1-(4-amino-2-hydroxyphenyl )-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one 
• 1448349-05-0 (E)-1-(4-amino-2-hydroxyphenyl)-3-(4-ethoxy-3-methoxyphenyl)prop-2-en-1-one 

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.

Porous coordination polymers of diverse topologies based on a twisted tetrapyridylbiaryl: Application as nucleophilic catalysts for acetylation of phenols

Porous coordination polymers (CPs) with partially uncoordinated pyridyl rings based on rationally designed polypyridyl linkers are appealing from the point of view of their application as nucleophilic catalysts. A D2d--symmetric tetradentate organic linker L, that is, 2,2 ',6,6'-tetramethoxy-3,3',5,5'-tetrakis(4-pyridyl)biphenyl, was designed and synthesized for metal-assisted self-assembly aimed at porous CPs. Depending on the nature of the metal ion and the counter anion, the ligand L is found to function as a 3- or 4-connecting building block leading to porous CPs of diverse topologies. The reaction of L with Zn(NO3)2 and Cd(NO3)2 yields porous 2D CPs of "fes" topology, in which the tetrapyridyl linker L serves as a 3-connecting unit with its free pyridyl rings well exposed into the pores. The functional utility of these porous CPs containing uncoordinated pyridyl rings is demonstrated by employing them as efficient heterogeneous nucleophilic catalysts for acetylation of a number of phenols with varying electronic properties and reactivities.