(Benzyloxycarbonylmethyl)triphenylphosphonium bromide manufacturers
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| | (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 | | EINECS: | | | Product Categories: | C-C Bond Formation;Olefination;Wittig Reagents | | Mol File: | 78385-36-1.mol |  |
| | (Benzyloxycarbonylmethyl)triphenylphosphonium bromide Chemical Properties |
| Melting point | 124 °C (dec.)(lit.) | | storage temp. | Storage temp. 2-8°C | | Appearance | White to off-white Solid |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 |
| | (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 bromide Preparation Products And Raw materials |
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