88607-72-1

Basic information

• Product Name: Acetic acid (S)-2-(4-acetoxy-phenyl)-7-methoxy-chroman-5-yl ester
• Synonyms: Acetic acid (S)-2-(4-acetoxy-phenyl)-7-methoxy-chroman-5-yl ester
• CAS NO: 88607-72-1
• Molecular Weight: 356.375
• Mol File: 88607-72-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid (S)-2-(4-acetoxy-phenyl)-7-methoxy-chroman-5-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (S)-2-(4-acetoxy-phenyl)-7-methoxy-chroman-5-yl ester(88607-72-1)
• EPA Substance Registry System: Acetic acid (S)-2-(4-acetoxy-phenyl)-7-methoxy-chroman-5-yl ester(88607-72-1)

Safety Data

• Hazardous Substances Data: 88607-72-1(Hazardous Substances Data)

Upstream product

• 520-29-6 (-)-(S)-sakuranetin 
• 480-41-1 naringenin 
• 3064-16-2 Acetic acid (S)-2-(4-acetoxy-phenyl)-7-methoxy-4-oxo-chroman-5-yl ester 

Downstream Products

• 161773-51-9 5-hydroxy-2-(4'-hydroxyphenyl)-7-methoxybenzopyrilium chloride 

Relevant articles and documents

Synthesis of 7-methoxyapigeninidin and its fungicidai activity against Gloeocercospora sorghi

In the structure of sakuranetin, which was isolated as a phytoalexin from the rice plant, the methoxy group at C-7 has been shown to be important for its high activity. Apigeninidin was isolated as a phytoalexin from sorghum, but it had no methoxy group at C-7. We prepared 7- methoxyapigeninidin and compared its fungicidal activity with that of apigeninidin. The 7-methoxyapigeninidin showed higher activity against sorghum fungi than apigeninidin, suggesting that the methoxy group at C-7 was important for the high fungicidal activity.