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419230 Aldrich

(Benzyloxycarbonylmethyl)triphenylphosphonium bromide

97%

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Properties

Related Categories C-C Bond Formation, Chemical Synthesis, Olefination, Synthetic Reagents, Wittig Reagents More...
InChI Key   AVQABZVTPWROCF-UHFFFAOYSA-M
assay   97%
mp   124 °C (dec.)(lit.)

Description

Packaging

10 g in glass bottle

Application

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

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles
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