213978-60-0

Basic information

• Product Name: 1,3-Dioxolane, 4-[2-[(4-methoxyphenyl)methoxy]ethyl]-2,2-dimethyl-, (4R)-
• CAS NO: 213978-60-0
• Molecular Formula: C15H22O4
• Molecular Weight: 266.337
• Mol File: 213978-60-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxolane, 4-[2-[(4-methoxyphenyl)methoxy]ethyl]-2,2-dimethyl-, (4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolane, 4-[2-[(4-methoxyphenyl)methoxy]ethyl]-2,2-dimethyl-, (4R)-(213978-60-0)
• EPA Substance Registry System: 1,3-Dioxolane, 4-[2-[(4-methoxyphenyl)methoxy]ethyl]-2,2-dimethyl-, (4R)-(213978-60-0)

Safety Data

• Hazardous Substances Data: 213978-60-0(Hazardous Substances Data)

Upstream product

• 5754-34-7 2-((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethanol 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 195257-62-6 (R)-2-(2-((4-methoxybenzyl)oxy)ethyl)oxirane 
• 1227373-79-6 (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-al 
• 1227374-12-0 (2S,4R,6S,8R)-10-(4-methoxybenzyloxy)-2,4,6,8-tetrakis(tert-butyldimethylsilyloxy)decan-1-ol 
• 1227373-90-1 1-(((3R,5S,7R,9S)-3,5,7,9,10-pentakis(tert-butyldimethylsilyloxy)decyloxy)methyl)-4-methoxybenzene 
• 1227374-11-9 (3R,7S,9S)-1-(4-methoxybenzyloxy)-7,9,10-tris(tert-butyldimethylsilyloxy)-3-hydroxy-decan-5-one 
• 1227373-89-8 (R)-1-(2-((2S,4S)-2,4,5-tris(tert-butyldimethylsilyloxy)pentyl)-1,3-dithian-2-yl)-4-(4-methoxybenzyloxy)butan-2-ol 
• 213978-45-1 (2R)-tert-butyl-[2-methoxy-4-(4-methoxybenzyloxy)-butoxy]-diphenylsilane 
• 213978-62-2 (2R)-1-(tert-butyldiphenylsilanyloxy)-4-(4-methoxybenzyloxy)-butan-2-ol 
• 213978-61-1 (2R)-4-(4-methoxybenzyloxy)-butane-1,2-diol 

Relevant articles and documents

Synthetic studies towards phorboxazole A. A convergent synthesis of the C31-C46 polyene oxane-hemiacetal side chain

A convergent and stereoselective synthesis of the C31-C46 side chain unit in the marine natural product phorboxazole A, which accommodates five asymmetric centres, three carbon-to-carbon double bonds and an oxane- hemiacetal unit, is described.

Fluorous mixture synthesis of four stereoisomers of the C21-C40 fragment of tetrafibricin

Four stereoisomers of the C21-C40 fragment are synthesized in a single exercise with the aid of fluorous tagging to encode configurations at C37 and C33. After demixing and detagging, the isomers were found to have substantially identical 1H NM