5466-90-0

Basic information

• Product Name: 2-PHTHALIMIDOETHYL ACETATE
• Synonyms: 2-PHTHALIMIDOETHYL ACETATE;TIMTEC-BB SBB007837;1H-Isoindole-1,3(2H)-dione, 2-[2-(acetyloxy)ethyl]-;2-[2-(acetyloxy)ethyl]-1h-isoindole-3(2h)-dione;N-(beta-Acetoxyethyl)phthalimide;N-ACETOXYETHYL PHTHALIMIDE;N-(2-ACETOXYETHYL)PHTHALIMIDE;2-(1,3(2H)-dioxo-1H-isoindol-2-yl)ethyl acetate
• CAS NO: 5466-90-0
• Molecular Formula: C₁₂H₁₁NO₄
• Molecular Weight: 233.22
• EINECS: 226-777-8
• Product Categories: Aromatics;Heterocycles;Miscellaneous Reagents
• Mol File: 5466-90-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 366.1 °C at 760 mmHg
• Flash Point: 175.2 °C
• Appearance: /
• Density: 1.32 g/cm³
• Vapor Pressure: 1.5E-05mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: 2-PHTHALIMIDOETHYL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHTHALIMIDOETHYL ACETATE(5466-90-0)
• EPA Substance Registry System: 2-PHTHALIMIDOETHYL ACETATE(5466-90-0)

Safety Data

• Hazardous Substances Data: 5466-90-0(Hazardous Substances Data)

Usage

Chemical Properties

White Cyrstalline Solid

InChI:InChI=1/C12H11NO4/c1-8(14)17-7-6-13-11(15)9-4-2-3-5-10(9)12(13)16/h2-5H,6-7H2,1H3

Upstream product

• 3891-07-4 N-(2-Hydroxyethyl)phthalimide 
• 108-24-7 acetic anhydride 
• 574-98-1 2-(2-bromoethyl)isoindoline-1,3-dione 
• 2466-76-4 N-Acetylimidazole 
• 506-96-7 Acetyl bromide 
• 141-78-6 ethyl acetate 
• 55694-50-3 N-(2-tetrahydropyran-2-yloxy-ethyl)-phthalimide 
• 123-91-1 1,4-dioxane 
• 85-44-9 phthalic anhydride 
• 20583-42-0 acetic acid-(2-phthalimido-vinyl ester) 
• 1120-64-5 2-methyl-4,5-dihydro-1,3-oxazole 
• 20622-86-0 N-(1,2-Dibromethyl)phthalimid 
• 20583-41-9 N-(1,2-diacetoxy-ethyl)-phthalimide 

Downstream Products

• 3485-84-5 N-vinylphthalimide 

Relevant articles and documents

One-step transformation of tetrahydropyranyl ethers using indium(III) triflate as the catalyst

A convergent one-step transformation of tetrahydropyranyl (THP) ethers is described. According to our earlier experiments, indium(III) triflate has proven to be an efficient catalyst for the transformation of THP ethers into their corresponding acetates.

Transesterification of α-substituted esters mediated by potassium carbonate

α-Substituted esters were efficiently and easily transesterificated at room temperature in the presence of potassium carbonate. α-Halo esters can be transesterificated without substitution of the halogen atom.

Solid state acetylation with acetylimidazole: Selective protection of primary alcohols and phenols

Primary alcohols and phenols have been acetylated with acetylimidazole by the solid state reaction, grinding both substrates with a pestle in a mortar.