18600-54-9

Basic information

• Product Name: AURORA 5332
• Synonyms: AURORA 5332;2-(4-METHYLPHENYL)-4H-3,1-BENZOXAZIN-4-ONE;BUTTPARK 160\40-93;2-(P-TOLYL)-3,1-BENZOXAZIN-4(4H)-ONE
• CAS NO: 18600-54-9
• Molecular Formula: C₁₅H₁₁NO₂
• Molecular Weight: 237.25
• Mol File: 18600-54-9.mol
• Article Data: 42

Chemical Properties

• Boiling Point: 359.4°Cat760mmHg
• Flash Point: 162.8°C
• Appearance: /
• Density: 1.2g/cm³
• Vapor Pressure: 2.39E-05mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: AURORA 5332(CAS DataBase Reference)
• NIST Chemistry Reference: AURORA 5332(18600-54-9)
• EPA Substance Registry System: AURORA 5332(18600-54-9)

Safety Data

• Hazardous Substances Data: 18600-54-9(Hazardous Substances Data)

Usage

General Description

AURORA 5332 is a chemical compound consisting of a mix of polyethylene glycol and polypropylene glycol. It is a non-ionic surfactant that is commonly used in various industrial, agricultural, and household applications. Its properties including high solvency, low foaming, and excellent wetting and dispersing abilities make it ideal for use in formulation of cleaners, detergents, and other chemical products. It is also used as an emulsifier, lubricant, and anti-static agent, and can be found in products such as paints, coatings, adhesives, and textiles. AURORA 5332 is considered a biodegradable and environmentally friendly option compared to other chemical surfactants.

InChI:InChI=1/C15H11NO2/c1-10-6-8-11(9-7-10)14-16-13-5-3-2-4-12(13)15(17)18-14/h2-9H,1H3

Upstream product

• 85-55-2 2-(4-toluoyl)benzoic acid 
• 325471-57-6 2-((4-methylbenzylidene)amino)benzoic acid 
• 104-87-0 4-methyl-benzaldehyde 
• 118-92-3 anthranilic acid 
• 1431097-93-6 C₁₅H₁₂INO₂ 
• 551-93-9 2-aminoacetophenone 
• 874-60-2 4-methyl-benzoyl chloride 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 
• 1373758-54-3 3-(4-methylphenyl)-5H-1,4,2-dioxazol-5-one 
• 2318-82-3 N-hydroxy-4-methylbenzamide 
• 201230-82-2 carbon monoxide 
• 624-31-7 4-tolyl iodide 
• 615-43-0 2-iodophenylamine 
• 153172-69-1 N-(2-cyanophenyl)-4-methylbenzamide 

Downstream Products

• 35709-65-0 2-(4-methylbenzoylamino)benzoylhydrazine 
• 88184-99-0 2-(p-methylphenyl)-3,4-dihydro-5H-1,3,4-benzotriazepin-5-one 
• 63002-95-9 3-amino-2-(4-methylphenyl)quinazolin-4(3H)-one 
• 244032-52-8 3-(2-amino-phenyl)-2-p-tolyl-3H-quinazolin-4-one 
• 67796-02-5 4-oxo-2-(p-tolyl)quinazoline-3(4H)-carbothioamide 
• 1464831-58-0 3-methyl-5-phenylindazolo[3,2-b]quinazolin-7(5H)-one 
• 63002-74-4 3-anilino-2-p-tolyl-3H-quinazolin-4-one 
• 1236769-21-3 3-(3-aminoethyl)-2-(4-methylphenyl)quinazolin-4(3H)-one 

Relevant articles and documents

Design, synthesis and anticonvulsant evaluation of N-[(substituted 1H-pyrazol-3-yl)amino]-2-(4-methylphenyl)quinazolin-4(3H)-one derivatives

A series of quinazolinone derivatives (7a-7e) have been designed, synthesized and evaluated for the anticonvulsant activity using maximal electroshock seizure (MES) model. The compound 3-[(5-(4-chloro)phenyl-4,5-dihydro-1H-pyrazol-3-yl)amino]-2-(4-methylphenyl)quinazolin-4(3H)-one (7c) was found to be most active compound showing 85.23 % protection and was found to be nonneurotoxic up to 4 h. This study indicates that the quinazolinone based derivatives could be further exploited for the discovery of newer and more effective anticonvulsant agents.

Recyclable Heterogeneous Palladium-Catalyzed Carbonylative Cyclization of 2-Iodoanilines with Aryl Iodides Leading to 2-Arylbenzoxazinones

A highly efficient and practical heterogeneous palladium-catalyzed carbonylative coupling of 2-iodoanilines with aryl iodides has been developed. The reaction occurs smoothly in toluene at 110 °C with N, N -diisopropylethylamine as base under carbon monoxide (5 bar) and offers a general and powerful tool for the construction of various valuable 2-arylbenzoxazinones with excellent atom-economy, high functional group tolerance, good to high yields, and easy recyclability of the palladium catalyst. The reaction is the first example of heterogeneous palladium-catalyzed carbonylative coupling for the preparation of diverse 2-arylbenzoxazinones from commercially easily available 2-iodoanilines and aryl iodides.

Palladium (0)-catalyzed C(sp2)-H oxygenation with carboxylic acids

Palladium (0)-catalyzed Ortho-benzoxylation of the sp2 C–H bond of arylbenzoxazinones with carboxylic acid is reported. With benzoxazinone as directing group, the reaction went smoothly under the benign condition and gave the desired product wi