78385-36-1

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78385-36-1 Structure

Identification	Back Directory
[Name] (Benzyloxycarbonylmethyl)triphenylphosphonium bromide
[CAS] 78385-36-1
[Synonyms] triphenyl benzoxycarbonyl Methyl phosphon (benzyloxycarbonylmethyl)triphenyl-phosphonium br triphenyl benzoxycarbonyl Methyl phosphoniuM broMide (BENZYLOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE (2-(Benzyloxy)-2-oxoethyl)triphenylphosphonium bromide [2-oxo-2-(benzyloxy)ethyl]triphenyl-phosphonium bromide (2-oxo-2-phenylmethoxyethyl)-triphenylphosphonium bromide (Benzyloxycarbonylmethyl)triphenylphosphonium bromide, 98 % 2-oxo-2-(phenylmethoxy)ethyl]triphenyl-Phosphonium bromide (1:1) Phosphonium, [2-oxo-2-(phenylmethoxy)ethyl]triphenyl-, bromide (1:1)
[Molecular Formula] C27H24BrO2P
[MDL Number] MFCD00191780
[MOL File] 78385-36-1.mol
[Molecular Weight] 491.36

Chemical Properties	Back Directory
[Melting point ] 124 °C (dec.)(lit.)

Safety Data	Back Directory
[Symbol(GHS) ] GHS07
[Signal word ] Warning
[Hazard statements ] H315-H319-H335
[Precautionary statements ] P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ] Xi
[Risk Statements ] 36/37/38
[Safety Statements ] 26-36
[WGK Germany ] 3

Hazard Information	Back Directory
[Uses] Reactant for: Atypical aza-Morita-Baylis-Hillman mechanism Thermal decomposition Double aza-Michael reaction Cyclodextrin derivatives Stereoselective preparation of α,β-unsaturated carbonyl compounds via stereoselective Wittig olefination with aldehydes under solventless conditions or ultrasonication Synthesis of [difluoro(alkenylphenyl)methyl]phosphonic acids on non-crosslinked polystyrene as inhibitors of PTP-1B via Wittig reaction
[reaction suitability] reaction type: C-C Bond Formation

Spectrum Detail	Back Directory
[Spectrum Detail] (Benzyloxycarbonylmethyl)triphenylphosphonium bromide(78385-36-1)FT-IR (Benzyloxycarbonylmethyl)triphenylphosphonium bromide(78385-36-1)IR

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