5198-46-9

Basic information

• Product Name: 3-(4-Methylphenyl)-1,3-oxazolidin-2-one
• Synonyms: 3-(4-Methylphenyl)-1,3-oxazolidin-2-one
• CAS NO: 5198-46-9
• Molecular Formula: C₁₀H₁₁NO₂
• Molecular Weight: 177.2
• Mol File: 5198-46-9.mol
• Article Data: 21

Chemical Properties

• Melting Point: 91 °C
• Boiling Point: 287.9°C at 760 mmHg
• Flash Point: 127.9°C
• Appearance: /
• Density: 1.199g/cm³
• Vapor Pressure: 0.00242mmHg at 25°C
• Refractive Index: 1.568
• PKA: 0.75±0.20(Predicted)
• CAS DataBase Reference: 3-(4-Methylphenyl)-1,3-oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-Methylphenyl)-1,3-oxazolidin-2-one(5198-46-9)
• EPA Substance Registry System: 3-(4-Methylphenyl)-1,3-oxazolidin-2-one(5198-46-9)

Safety Data

• Hazardous Substances Data: 5198-46-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H11NO2/c1-8-2-4-9(5-3-8)11-6-7-13-10(11)12/h2-5H,6-7H2,1H3

Upstream product

• 96-49-1 [1,3]-dioxolan-2-one 
• 106-49-0 p-toluidine 
• 74552-28-6 N-(p-Tolyl)carbamidsaeure-β-chlorethylester 
• 497-25-6 dimethylenecyclourethane 
• 106-38-7 para-bromotoluene 
• 5720-05-8 4-methylphenylboronic acid 
• 624-31-7 4-tolyl iodide 
• 14618-59-8 N-(tert-butoxycarbonyl)-4-methylaniline 
• 75-21-8 oxirane 
• 124-38-9 carbon dioxide 
• 5602-93-7 ethyl (2-hydroxyethyl)carbamate 
• 627-11-2 2-Chloroethyl chloroformate 
• 106-93-4 ethylene dibromide 
• 107-06-2 1,2-dichloro-ethane 

Downstream Products

• 1077-24-3 3-(p-tolylamino)propionitrile 
• 1313524-82-1 C₁₆H₁₃ClFNO₂ 
• 1313524-81-0 C₁₆H₁₃F₂NO₂ 
• 1313524-80-9 C₁₆H₁₃Cl₂NO₂ 
• 2933-74-6 2-[(4-methylphenyl)amino]-ethanol 
• 28690-22-4 3-(p-tolyl)thiazolidin-2-one 
• 71472-58-7 3,4-dihydro-7-methyl-2H-1,4-benzoxazine 

Relevant articles and documents

Room Temperature Cu-Catalyzed N-Arylation of Oxazolidinones and Amides with (Hetero)Aryl Iodides

N,N′-Bis(pyridin-2-ylmethyl)oxalamide (BPMO) was found to be an apposite promoter for the Cu-catalyzed N-arylation of oxazolidinones and primary and secondary amides with (hetero)aryl iodides at room temperature. Excellent chemoselectivity reached between

METHODS FOR PREPARING BENZOXAZINES

A method is provided for preparing a compound / the method comprising carrying out the following reaction: Formula (i); Formula (ii) where: R10 is hydrogen or a hydroxy protecting group; PG is an amine protecting group; and q is 1 where PG is a

Synthesis of Oxazolidinones and Derivatives through Three-Component Fixation of Carbon Dioxide

An effective three-component fixation of atmospheric CO2 with readily available 1,2-dichloroethane and aromatic amine toward oxazolidinones catalyzed by in situ NHC was developed. The reaction occurred in good to excellent yields with good gene