79388-03-7

Basic information

• Product Name: Ethyl 2-ethyl-4-oxo-4H-chroMene-3-carboxylate
• Synonyms: Ethyl 2-ethyl-4-oxo-4H-chroMene-3-carboxylate
• CAS NO: 79388-03-7
• Molecular Formula: C14H14O4
• Molecular Weight: 246.25856
• Mol File: 79388-03-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Ethyl 2-ethyl-4-oxo-4H-chroMene-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2-ethyl-4-oxo-4H-chroMene-3-carboxylate(79388-03-7)
• EPA Substance Registry System: Ethyl 2-ethyl-4-oxo-4H-chroMene-3-carboxylate(79388-03-7)

Safety Data

• Hazardous Substances Data: 79388-03-7(Hazardous Substances Data)

Upstream product

• 2009-98-5 ethyl propionyl-2-diazoacetate 
• 90-02-8 salicylaldehyde 
• 4949-44-4 ethyl propanoylacetate 
• 5538-51-2 O-acetylsalicyloyl chloride 
• 393-52-2 2-Fluorobenzoyl chloride 
• 92397-14-3 (E)-2-(2-Acetoxy-benzoyl)-3-hydroxy-pent-2-enoic acid ethyl ester 

Relevant articles and documents

Cp?Ir(III)-Catalyzed C-H/O-H Functionalization of Salicylaldehydes for the Synthesis of Chromones at Room Temperature

Herein, we report Cp Ir(III)-catalyzed C-H/O-H-bond functionalization of salicylaldehydes with α-diazocarbonyl compounds for the synthesis of chromones under redox-neutral conditions. The reaction proceeds at room temperature and displays excellent functi

Synthesis of Benzopyranoisoxazol-4-ones from 2-Substituted Chromone-3-carboxylic Esters. A Reinvestigation of the Reaction of 3-Acetyl-4-hydroxycoumarins with Hydroxylamine. Synthesis of 4-(2-Hydroxybenzoyl)isoxazol-5-ones

A convenient method for the synthesis of ethyl 2-substituted chromone-3-carboxylates by the condensation of o-acetoxyaroyl chlorides with β-keto esters is described.These chromones are converted into the corresponding 4H-benzopyranoisoxazol-4-on