202390-90-7

Basic information

• Product Name: 2-(1,4-Dioxa-spiro[4.5]dec-7-en-8-yl)-4-(2-iodo-5-methoxy-phenyl)-butyric acid methyl ester
• Synonyms: 2-(1,4-Dioxa-spiro[4.5]dec-7-en-8-yl)-4-(2-iodo-5-methoxy-phenyl)-butyric acid methyl ester
• CAS NO: 202390-90-7
• Molecular Weight: 472.32
• Mol File: 202390-90-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(1,4-Dioxa-spiro[4.5]dec-7-en-8-yl)-4-(2-iodo-5-methoxy-phenyl)-butyric acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1,4-Dioxa-spiro[4.5]dec-7-en-8-yl)-4-(2-iodo-5-methoxy-phenyl)-butyric acid methyl ester(202390-90-7)
• EPA Substance Registry System: 2-(1,4-Dioxa-spiro[4.5]dec-7-en-8-yl)-4-(2-iodo-5-methoxy-phenyl)-butyric acid methyl ester(202390-90-7)

Safety Data

• Hazardous Substances Data: 202390-90-7(Hazardous Substances Data)

Upstream product

• 225526-36-3 2-(2-(2-Bromo-5-methoxyphenyl)ethoxy)tetrahydropyran 
• 139469-06-0 1-bromo-5-dimethoxy-2-vinylbenzene 
• 75534-35-9 2-(2-bromo-5-methoxyphenyl)ethan-1-ol 
• 72594-56-0 2-(2-Iodo-5-methoxy-phenyl)-ethanol 
• 72594-60-6 1-Iodo-2-(2-iodo-ethyl)-4-methoxy-benzene 
• 172270-85-8 8-(methoxyformylmethylene)-1,4-dioxaspiro[4.5]decane 

Downstream Products

• 202390-91-8 2-(1,4-Dioxa-spiro[4.5]dec-7-en-8-yl)-4-(2-iodo-5-methoxy-phenyl)-butan-1-ol 

Relevant articles and documents

Synthesis of a phenolic analog of aphidicolin. Diminished stereoselection in intramolecular 6-exo Heck reactions of substrates having a hydrocarbon tether

Spirotetracycle 14, generated by intramolecular Heck cyclization of 13, was converted to the phenolic analog 20 of aphidicolin. That the nature of the tether connecting insertion partners can dramatically alter diastereoselection in intramolecular Heck reactions is also demonstrated.