132260-57-2

Basic information

• Product Name: 4,6-bis<<(2-methoxyethoxy)methyl>oxy>-2-iodobenzoic acid
• Synonyms: 4,6-bis<<(2-methoxyethoxy)methyl>oxy>-2-iodobenzoic acid
• CAS NO: 132260-57-2
• Molecular Weight: 456.231
• Mol File: 132260-57-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4,6-bis<<(2-methoxyethoxy)methyl>oxy>-2-iodobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-bis<<(2-methoxyethoxy)methyl>oxy>-2-iodobenzoic acid(132260-57-2)
• EPA Substance Registry System: 4,6-bis<<(2-methoxyethoxy)methyl>oxy>-2-iodobenzoic acid(132260-57-2)

Safety Data

• Hazardous Substances Data: 132260-57-2(Hazardous Substances Data)

Upstream product

• 132260-55-0 methyl 4,6-dihydroxy-2-iodobenzoate 
• 132260-54-9 N,N-diethyl-4,6-bis<(tert-butyldimethylsilyl)oxy>-2-iodobenzamide 
• 132260-53-8 N,N-diethyl 2,4-bis<(tert-butyldimethylsilyl)oxy>benzamide 
• 132297-26-8 methyl 2,4-bis<(tert-butyldimethylsilyl)oxy>benzoate 
• 2150-47-2 methyl 2,4-dihydroxybenzoate 
• 132260-56-1 methyl 4,6-bis<<(2-methoxyethoxy)methyl>oxy>-2-iodobenzoate 

Downstream Products

• 17924-92-4 zearalenone 

Relevant articles and documents

Synthesis of β-Resorcylic Macrolides via Organopalladium Chemistry. Application to the Total Synthesis of (S)-Zearalenone

The β-resorcyclic macrolides are a class of naturally occurring 12- and 14-membered macrolides.Zearalenone (1), a 14-membered macrolide of this type, displays useful biological activity, which has led to great synthetic interest.In this paper the intramolecular coupling reaction of an organostannane with an electrophile is used to construct β-resorcylic macrolides.The intramolecular coupling of an aryl iodide with a vinylstannane provided the highest yield of lactones.This methodology was then used to prepare (S)-zearalenone (1).