59636-00-9

Basic information

• Product Name: Phosphonium, [[2-(ethoxycarbonyl)phenyl]methyl]triphenyl-, bromide
• CAS NO: 59636-00-9
• Molecular Formula: C28H26O2P.Br
• Molecular Weight: 505.391
• Mol File: 59636-00-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phosphonium, [[2-(ethoxycarbonyl)phenyl]methyl]triphenyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonium, [[2-(ethoxycarbonyl)phenyl]methyl]triphenyl-, bromide(59636-00-9)
• EPA Substance Registry System: Phosphonium, [[2-(ethoxycarbonyl)phenyl]methyl]triphenyl-, bromide(59636-00-9)

Safety Data

• Hazardous Substances Data: 59636-00-9(Hazardous Substances Data)

Upstream product

• 87-24-1 ethyl 2-methylbenzoate 
• 603-35-0 triphenylphosphine 
• 7115-91-5 2-ethoxycarbonylbenzyl bromide 

Downstream Products

• 143366-19-2 2-[(E)-3-Methoxycarbonyl-2-trifluoromethyl-1-(triphenyl-λ⁵-phosphanylidene)-allyl]-benzoic acid ethyl ester 
• 143366-12-5 2-{(Z)-3,3,3-Trifluoro-2-[methoxycarbonyl-(triphenyl-λ⁵-phosphanylidene)-methyl]-propenyl}-benzoic acid ethyl ester 
• 143366-20-5 2-[3,3,4,4,5,5,5-Heptafluoro-2-[1-methoxycarbonyl-meth-(E)-ylidene]-1-(triphenyl-λ⁵-phosphanylidene)-pentyl]-benzoic acid ethyl ester 
• 143366-13-6 2-{(Z)-3,3,4,4,5,5,5-Heptafluoro-2-[methoxycarbonyl-(triphenyl-λ⁵-phosphanylidene)-methyl]-pent-1-enyl}-benzoic acid ethyl ester 
• 98459-88-2 2-[(Z)-2-(12-Fluoro-benzo[c]phenanthren-2-yl)-vinyl]-benzoic acid ethyl ester 
• 98460-00-5 2-[(E)-2-(11-Fluoro-dibenzo[c,g]phenanthren-9-yl)-vinyl]-benzoic acid ethyl ester 
• 864850-65-7 benzyl 2-[2-[2-(ethoxycarbonyl)phenyl]-1-ethenyl]benzoate 
• 90011-52-2 ethyl 2-(2-nitrostyryl)benzoate 
• 593248-91-0 2-[2-(2-ethoxycarbonylphenyl)-1-ethyl]benzoic acid 
• 67504-57-8 (1SR,1aRS,6aRS)-1-phenyl-1,1a,6,6a-tetrahydrocyclopropa[α]indene 
• 83640-57-7 (E)-2-<2-(N-methylindol-3-yl)ethenyl>benzoic acid 
• 345630-05-9 Ethyl cis-2-<2-(4-nitrophenyl)ethenyl>benzoate 

Relevant articles and documents

Synthesis of 6H-isoindolo[2,1-a]indol-6-ones through wittig reaction and tandem reductive cyclization-lactamization

A convenient and efficient two-step route to 6H-Isoindolo[2,1-a]indol-6- ones has been developed starting from o-nitrobenzaldehydes. The methodology involves Wittig reaction followed by tandem reductive cyclization-lactamization. A series of isoindoloindo

A convenient synthesis of methyl 1-alkoxy-3-perfluoroalkyl-2-naphthoates

Methyl 1-alkoxy-3-perfluoroalkyl-2-naphthoates 5 were synthesized by heating appropriately substituted 2-triphenylphosphoranylidene-2-butenoates 3 in xylenes at 250°C in a sealed tube. Compounds 3 were obtained via an intramolecular Wittig reaction of 2-alkoxycarbonylbenzyltriphenylphosphonium bromide (1) with methyl 2-perfluoroalkynoates 2 in the presence of potassium carbonate.

Microbicidal nitrofuryl compounds

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