419230
(Benzyloxycarbonylmethyl)triphenylphosphonium bromide
97%
About This Item
Recommended Products
assay
97%
reaction suitability
reaction type: C-C Bond Formation
mp
124 °C (dec.) (lit.)
SMILES string
[Br-].O=C(C[P+](c1ccccc1)(c2ccccc2)c3ccccc3)OCc4ccccc4
InChI
1S/C27H24O2P.BrH/c28-27(29-21-23-13-5-1-6-14-23)22-30(24-15-7-2-8-16-24,25-17-9-3-10-18-25)26-19-11-4-12-20-26;/h1-20H,21-22H2;1H/q+1;/p-1
InChI key
AVQABZVTPWROCF-UHFFFAOYSA-M
Application
- 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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service