851009-33-1

Basic information

• Product Name: 5,7-Decadienoic acid, 10-[(4-methoxyphenyl)methoxy]-7-methyl-, methyl ester, (5E,7E)-
• CAS NO: 851009-33-1
• Molecular Formula: C20H28O4
• Molecular Weight: 332.44
• Mol File: 851009-33-1.mol

Chemical Properties

• CAS DataBase Reference: 5,7-Decadienoic acid, 10-[(4-methoxyphenyl)methoxy]-7-methyl-, methyl ester, (5E,7E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 5,7-Decadienoic acid, 10-[(4-methoxyphenyl)methoxy]-7-methyl-, methyl ester, (5E,7E)-(851009-33-1)
• EPA Substance Registry System: 5,7-Decadienoic acid, 10-[(4-methoxyphenyl)methoxy]-7-methyl-, methyl ester, (5E,7E)-(851009-33-1)

Safety Data

• Hazardous Substances Data: 851009-33-1(Hazardous Substances Data)

Upstream product

• 500702-36-3 (2E)-2-iodo-5-[(4-methoxybenzyl)oxy]pent-2-ene 

Downstream Products

• 851009-46-6 (2Z,8E,10E)-1-(tert-butyldimethylsilyloxy)-5-(tert-butyldiphenylsilyloxy)-13-(4-methoxybenzyloxy)-10-methyldeca-2,8,10-trien-4-one 
• 851009-38-6 (2E,8E,10E)-1-benzyloxy-5-(tert-butyldiphenylsilyloxy)-13-(4-methoxybenzyloxy)-10-methyltrideca-2,8,10-trien-4-one 
• 851009-35-3 (6E,8E)-3-(tert-butyldiphenylsilyloxy)-11-(4-methoxybenzyloxy)-8-methyl-2-oxoundeca-6,8-dienyldimethylphosphonate 
• 851009-45-5 (5E,7E)-2-(tert-butyldiphenylsilyloxy)-10-(4-methoxybenzyloxy)-7-methyldeca-5,7-dienoic acid methoxy(methyl)amide 
• 851009-44-4 (5E,7E)-2-(tert-Butyl-diphenyl-silanyloxy)-10-(4-methoxy-benzyloxy)-7-methyl-deca-5,7-dienoic acid methyl ester 
• 851009-40-0 (2E,8E,10E)-1-acetoxy-13-(4-methoxybenzyloxy)-10-methyltrideca-2,8,10-trien-4-one 
• 851009-55-7 (6E,8E)-11-(4-methoxybenzyloxy)-8-methyl-2-oxoundeca-6,8-dienyldimethylphosphonate 
• 851009-34-2 (5E,7E)-2-hydroxy-10-(4-methoxybenzyloxy)-7-methyldeca-5,7-dienoic acid methyl ester 

Relevant articles and documents

Stereoselective synthesis of the octahydronaphthalene unit of integramycin via an intramolecular Diels-Alder reaction

(Chemical Equation Presented). The racemic cis-decalin core fragment 30 of integramycin was synthesized by a sequence involving a highly diastereoselective intramolecular Diels-Alder reaction of triene 24. A remarkable switch in stereoselectivity occurred