2043-21-2

Basic information

• Product Name: 3-ACRYLOYL-2-OXAZOLIDINONE
• Synonyms: 3-ACRYLOYL-2-OXAZOLIDINONE;Acryloyl-2-oxazolidinone;3-Acryloyloxazolidin-2-one
• CAS NO: 2043-21-2
• Molecular Formula: C₆H₇NO₃
• Molecular Weight: 141.12
• Mol File: 2043-21-2.mol
• Article Data: 16

Chemical Properties

• Melting Point: 83 °C
• Boiling Point: 194.48 °C at 760 mmHg
• Flash Point: 71.419 °C
• Appearance: /
• Density: 1.281 g/cm³
• Vapor Pressure: 0.441mmHg at 25°C
• Refractive Index: 1.505
• Storage Temp.: Refrigerator
• PKA: -1.76±0.20(Predicted)
• CAS DataBase Reference: 3-ACRYLOYL-2-OXAZOLIDINONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ACRYLOYL-2-OXAZOLIDINONE(2043-21-2)
• EPA Substance Registry System: 3-ACRYLOYL-2-OXAZOLIDINONE(2043-21-2)

Safety Data

• Hazardous Substances Data: 2043-21-2(Hazardous Substances Data)

Usage

General Description

3-Acryloyl-2-oxazolidinone is a chemical compound with the molecular formula C7H9NO2. It is a white to yellow crystalline substance that is commonly used as a monomer for the production of polymers. 3-ACRYLOYL-2-OXAZOLIDINONE is known for its reactivity and can undergo various types of chemical reactions, including polymerization and cross-linking, making it useful in the manufacturing of coatings, adhesives, and other industrial applications. Additionally, 3-Acryloyl-2-oxazolidinone has been studied for its potential use in biomedical applications, such as drug delivery systems and tissue engineering, due to its biocompatibility and ability to form stable polymer networks. However, it is important to handle this compound with caution as it may cause irritation to the skin, eyes, and respiratory system upon exposure.

InChI:InChI=1/C6H7NO3/c1-2-5(8)7-3-4-10-6(7)9/h2H,1,3-4H2

Upstream product

• 497-25-6 dimethylenecyclourethane 
• 814-68-6 acryloyl chloride 
• 2051-76-5 acrylic acid anhydride 
• 625-36-5 2-chloropropionyl chloride 
• 15486-96-1 3-Bromopropionyl chloride 
• 68641-49-6 bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride 
• 79-10-7 acrylic acid 
• 1274906-21-6 3-[3-(benzyloxy)prop-1-yn-1-yl]-1,3-oxazolidin-2-one 
• 3282-30-2 pivaloyl chloride 

Downstream Products

• 116733-45-0 (1R)-3-[(cyclohex-3-enyl)-carbonyl]-1,3-oxazolidin-2-one 
• 116733-45-0 3-<(1R)-3-Cyclohexen-1-ylcarbonyl>-1,3-oxazolidin-2-one 
• 134178-48-6 3-(4-Cyclohex-1-enyl-pentanoyl)-oxazolidin-2-one 
• 121809-01-6 (-)-3-(7'-Benzyloxymethyl-bicyclo<2.2.1>hept-5'-ene-2'-carbonyl)-1,3-oxazolin-2-one 
• 121809-01-6 3-((1S,2R,4R,7S)-7-Benzyloxymethyl-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one 
• 145146-15-2 (R)-3-(3-cyclohexyl-2-(methylthio)cyclobut-3-enecarbonyl)-1,3-oxazolidin-2-one 
• 134166-10-2 (S)-3-(4-methylcyclohex-3-enecarbonyl)oxazolidin-2-one 
• 151153-99-0 3-[(4'-methylcyclohex-3'-ene-1'-yl)carbonyl]oxazolidin-2-one 
• 190083-62-6 Acetic acid (1S,6S)-3-methyl-6-(2-oxo-oxazolidine-3-carbonyl)-cyclohex-2-enyl ester 

Relevant articles and documents

P-Anisaldehyde-Photosensitized Sulfonylcyanation of Chiral Cyclobutenes: Enantioselective Access to Cyclic and Acyclic Systems Bearing All-Carbon Quaternary Stereocenters

The photosensitized p-Anisaldehyde-mediated addition of sulfonylcyanides onto the I -system of cyclobutenes is shown to afford highly functionalized cyclobutanes in high yields and diastereocontrol. The homochiral cyclobutene precursors are accessible on multigram scale in two steps through an asymmetric [2 + 2] cycloaddition/vinyl thioether reduction sequence. The enantiopure cyclobutylnitriles can be elaborated further through SmI2-mediated ring opening or converted into new enantiopure cyclobutenes through base-mediated sulfone elimination.

Asymmetric Diels-Alder Reaction of α,β-Unsaturated Oxazolidin-2-one Derivatives Catalyzed by a Chiral Fe(III)-Bipyridine Diol Complex

An asymmetric FeIII-bipyridine diol catalyzed Diels-Alder reaction of α,β-unsaturated oxazolidin-2-ones has been developed. Among various FeII/FeIII salts, Fe(ClO4)3·6H2O was selected as th

Gold-catalyzed rearrangement of propargylic tert-butyl carbonates

Diversely substituted 4-alkylidene-1,3-dioxolan-2-ones are efficiently synthesized by a gold(I)-catalyzed rearrangement of propargylic tert-butyl carbonates. The substrates are readily accessible and the transformation, which is performed under mild react