79344-53-9

Basic information

• Product Name: 4-Anilinomethyl-7-methoxycoumarin
• Synonyms: 4-Anilinomethyl-7-methoxycoumarin
• CAS NO: 79344-53-9
• Molecular Weight: 281.311
• Mol File: 79344-53-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-Anilinomethyl-7-methoxycoumarin(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Anilinomethyl-7-methoxycoumarin(79344-53-9)
• EPA Substance Registry System: 4-Anilinomethyl-7-methoxycoumarin(79344-53-9)

Safety Data

• Hazardous Substances Data: 79344-53-9(Hazardous Substances Data)

Upstream product

• 84105-42-0 4-Hydroxymethyl-6-methylcoumarin 
• 84096-84-4 6-methyl-2-oxo-2H-chromene-4-carbaldehyde 
• 14002-89-2 4,6-dimethyl-chromen-2-one 
• 35231-44-8 4-(bromomethyl)-7-methoxycoumarin 
• 62-53-3 aniline 
• 41295-65-2 4‐chloromethylene‐6‐methyl‐2H‐chromene‐2‐one 

Relevant articles and documents

Synthesis of 4-Substituted Coumarins, 3a,8a-Dihydrofurobenzofuran-2(3H)-ones and 2,3,3a,8a-Tetrahydrobenzofuropyrrol-2(1H)-ones

Oxidation of methylcoumarins (I) with SeO2 shows that the methyl group in position-4 is selectively oxidised to CHO but methyl groups in other positions remain unaffected.However, a bulky substituent in position-3 hampers oxidation of CH3 in position-4.A large number of derivatives (III to XIV) of II have been prepared by making use of the reactivity of CHO function. 3a,8a-Dihydrofurobenzofuran-2(3H)-ones (XVa-c) and 2,3,3a,8a-tetrahydrobenzofuropyrrol-2(1H)-ones (XVIa-c) have been synthesised by the action of zinc and acetic acid on II and III, respectively.