367526-66-7

Basic information

• Product Name: Ethyl 2,8-diMethyl-4-oxo-4H-chroMene-3-carboxylate
• Synonyms: Ethyl 2,8-diMethyl-4-oxo-4H-chroMene-3-carboxylate
• CAS NO: 367526-66-7
• Molecular Formula: C14H14O4
• Molecular Weight: 246.25856
• Mol File: 367526-66-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Ethyl 2,8-diMethyl-4-oxo-4H-chroMene-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2,8-diMethyl-4-oxo-4H-chroMene-3-carboxylate(367526-66-7)
• EPA Substance Registry System: Ethyl 2,8-diMethyl-4-oxo-4H-chroMene-3-carboxylate(367526-66-7)

Safety Data

• Hazardous Substances Data: 367526-66-7(Hazardous Substances Data)

Upstream product

• 141-97-9 ethyl acetoacetate 
• 824-42-0 2-methoxy-3-methylbenzaldehyde 
• 2009-97-4 ethyl 2-diazo-3-oxobutanoate 
• 27893-05-6 2-acetoxy-3-methyl-benzoyl chloride 
• 367526-59-8 ethyl [(2-acetoxy-3-methylphenyl)hydroxymethylidene]ethoxycarbonylacetate 
• 4386-39-4 3-methylaspirin 
• 83-40-9 3-methylsalicylic acid 

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

A highly practical route to 2-methylchromones from 2-acetoxybenzoic acids

2-Methylchromones were accessed via a keto ester condensation on 2-acetoxybenzoyl chloride, followed by cyclization and decarboxylation. No column chromatography was required in the process.