5944-33-2

Basic information

• Product Name: Phosphonium, [3-(2-methyl-1,3-dioxolan-2-yl)propyl]triphenyl-, bromide
• CAS NO: 5944-33-2
• Molecular Formula: C25H28O2P.Br
• Molecular Weight: 471.374
• Mol File: 5944-33-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phosphonium, [3-(2-methyl-1,3-dioxolan-2-yl)propyl]triphenyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonium, [3-(2-methyl-1,3-dioxolan-2-yl)propyl]triphenyl-, bromide(5944-33-2)
• EPA Substance Registry System: Phosphonium, [3-(2-methyl-1,3-dioxolan-2-yl)propyl]triphenyl-, bromide(5944-33-2)

Safety Data

• Hazardous Substances Data: 5944-33-2(Hazardous Substances Data)

Upstream product

• 24400-75-7 ethylene-cetal de la bromo-5 pentanone-2 
• 603-35-0 triphenylphosphine 
• 3884-71-7 bromo-5-pentanone-2 
• 517-23-7 3-acetyl-2-oxo-4,5-dihydrofuran 

Downstream Products

• 99481-22-8 2-<4-(4-benzyloxyphenyl)-3-pentenyl>-2-methyl-1,3-dioxolane 
• 117398-85-3 4-(2-Methyl-[1,3]dioxolan-2-yl)-2-(triphenyl-λ⁵-phosphanylidene)-butyric acid methyl ester 
• 99481-24-0 2-<4-(4-hydroxyphenyl)pentyl>-2-methyl-1,3-dioxolane 
• 117398-86-4 (E)-4-[(R)-4-((S)-3-Benzyloxy-1-hydroxy-propyl)-2-oxo-oxazolidin-3-yl]-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-but-2-enoic acid methyl ester 
• 117398-87-5 (E)-4-[(R)-4-((R)-3-Benzyloxy-1-iodo-propyl)-2-oxo-oxazolidin-3-yl]-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-but-2-enoic acid methyl ester 
• 213264-85-8 4-{2-Methoxy-5-[4-(2-methyl-[1,3]dioxolan-2-yl)-butyl]-phenoxy}-benzaldehyde 
• 213264-58-5 2-methyl-2-{5-[4-methoxy-3-(4-methoxycarbonyl-phenoxy)phenyl]-but-3-enyl}-1,3-dioxolan 
• 3054-93-1 [3-(2-Methyl-[1,3]dioxolan-2-yl)-propylidene]-triphenyl-λ⁵-phosphane 
• 115304-68-2 (S)-1,3-Dimethyl-2-[(1E,3Z)-3-methyl-6-(2-methyl-[1,3]dioxolan-2-yl)-hexa-1,3-dienyl]-4-oxo-cyclohex-2-enecarboxylic acid methyl ester 
• 115304-69-3 (S)-1,3-Dimethyl-2-[(1E,3E)-3-methyl-6-(2-methyl-[1,3]dioxolan-2-yl)-hexa-1,3-dienyl]-4-oxo-cyclohex-2-enecarboxylic acid methyl ester 

Relevant articles and documents

Selectivity in the hydrogenation of 20(22)-dehydro steroids

-

Implication of a Common Trimethylenemethane Intermediate in Dimer Formation and Structural Methylenecyclopropane Rearrangement of a Bicyclohex-1-ene to a 5-alkylidenebicyclopentane

Stereospecifically labelled 2,6,6-trimethylbicyclohex-1-ene (17b), generated by α-elimination from 1,1-dibromo-6-trans-trideuteriomethylhepta-1,5-diene (8b), dimerizes to stereospecifically labelled and products, 15b and 16b, and to