ChemicalBook > Product Catalog > Organic Chemistry > (Benzyloxycarbonylmethyl)triphenylphosphonium bromide
(Benzyloxycarbonylmethyl)triphenylphosphonium bromide
(Benzyloxycarbonylmethyl)triphenylphosphonium bromide Basic information
- Product Name:
- (Benzyloxycarbonylmethyl)triphenylphosphonium bromide
- Synonyms:
-
- (BENZYLOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE
- (Benzyloxycarbonylmethyl)triphenylphosphonium bromide, 98 %
- (benzyloxycarbonylmethyl)triphenyl-phosphonium br
- triphenyl benzoxycarbonyl Methyl phosphoniuM broMide
- (2-(Benzyloxy)-2-oxoethyl)triphenylphosphonium bromide
- [2-oxo-2-(benzyloxy)ethyl]triphenyl-phosphonium bromide
- triphenyl benzoxycarbonyl Methyl phosphon
- (2-oxo-2-phenylmethoxyethyl)-triphenylphosphonium bromide
- CAS:
- 78385-36-1
- MF:
- C27H24BrO2P
- MW:
- 491.36
- Product Categories:
-
- C-C Bond Formation
- Olefination
- Wittig Reagents
- Mol File:
- 78385-36-1.mol
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(Benzyloxycarbonylmethyl)triphenylphosphonium bromide Chemical Properties
- Melting point:
- 124 °C (dec.)(lit.)
- storage temp.
- Storage temp. 2-8°C
- Appearance
- White to off-white Solid
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MSDS
- Language:English Provider:SigmaAldrich
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(Benzyloxycarbonylmethyl)triphenylphosphonium bromide Usage And Synthesis
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
(Benzyloxycarbonylmethyl)triphenylphosphonium bromideSupplier
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(Benzyloxycarbonylmethyl)triphenylphosphonium bromide(78385-36-1)Related Product Information
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- (Benzyloxycarbonylmethyl)triphenylphosphonium bromide