397886-48-5

Basic information

• Product Name: 1,3-Dioxolane, 4-[(2R)-2-[(4-methoxyphenyl)methoxy]-4-pentenyl]-2,2-dimethyl-, (4S)-
• CAS NO: 397886-48-5
• Molecular Formula: C18H26O4
• Molecular Weight: 306.402
• Mol File: 397886-48-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxolane, 4-[(2R)-2-[(4-methoxyphenyl)methoxy]-4-pentenyl]-2,2-dimethyl-, (4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolane, 4-[(2R)-2-[(4-methoxyphenyl)methoxy]-4-pentenyl]-2,2-dimethyl-, (4S)-(397886-48-5)
• EPA Substance Registry System: 1,3-Dioxolane, 4-[(2R)-2-[(4-methoxyphenyl)methoxy]-4-pentenyl]-2,2-dimethyl-, (4S)-(397886-48-5)

Safety Data

• Hazardous Substances Data: 397886-48-5(Hazardous Substances Data)

Upstream product

• 87318-96-5 (4S)-4-((2R)-2-hydroxypent-4-enyl)-2,2-dimethyl-1,3-dioxolane 
• 2746-25-0 p-Methoxybenzyl bromide 

Downstream Products

• 397886-69-0 2,2-Dimethyl-propionic acid (3R,5S)-5-hydroxy-3-(4-methoxy-benzyloxy)-8-trimethylsilanyl-oct-7-ynyl ester 
• 397886-62-3 2,2-Dimethyl-propionic acid 2-[(2S,4R,6S)-6-[(2E,9E)-(6R,7R)-11-hydroxy-6-(4-methoxy-benzyloxy)-7-methyl-undeca-2,9-dien-4-ynyl]-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-ethyl ester 
• 397886-66-7 2,2-Dimethyl-propionic acid (2S,4R)-2-methanesulfonyloxy-4-(4-methoxy-benzyloxy)-hept-6-enyl ester 
• 397886-54-3 2,2-Dimethyl-propionic acid (3R,5S)-5-hydroxy-3-(4-methoxy-benzyloxy)-oct-7-ynyl ester 
• 397886-46-3 2,2-Dimethyl-propionic acid 2-[(2S,4R,6S)-6-((E)-3-iodo-allyl)-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-ethyl ester 
• 397886-55-4 2,2-Dimethyl-propionic acid 2-[(2S,4R,6S)-2-(4-methoxy-phenyl)-6-prop-2-ynyl-[1,3]dioxan-4-yl]-ethyl ester 
• 397886-50-9 2,2-Dimethyl-propionic acid (2S,4R)-2-hydroxy-4-(4-methoxy-benzyloxy)-hept-6-enyl ester 
• 397886-52-1 2,2-Dimethyl-propionic acid (R)-3-(4-methoxy-benzyloxy)-4-(R)-oxiranyl-butyl ester 
• 397886-51-0 (R)-2-[(R)-2-(4-Methoxy-benzyloxy)-pent-4-enyl]-oxirane 

Relevant articles and documents

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Chemical equation presented A convergent, highly enantioselective synthesis of the fully functionalized AB sector of cochleamycin A is described. A pair of building blocks, crafted from L-malic and L-ascorbic acids, are conjoined in a manner that gives ri