389196
(3-Benzyloxypropyl)triphenylphosphonium bromide
98%
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About This Item
reaction suitability
core: phosphonium, reaction type: C-C Bond Formation
mp
153-154 °C (lit.)
functional group
ether, phenyl, phosphine
InChI
1S/C28H28OP.BrH/c1-5-14-25(15-6-1)24-29-22-13-23-30(26-16-7-2-8-17-26,27-18-9-3-10-19-27)28-20-11-4-12-21-28;/h1-12,14-21H,13,22-24H2;1H/q+1;/p-1
SMILES string
[Br-].C(COCc1ccccc1)C[P+](c2ccccc2)(c3ccccc3)c4ccccc4
InChI key
DWYCJWXMZGVGJV-UHFFFAOYSA-M
assay
98%
Quality Level
form
powder
Related Categories
Application
- Spirocyclohexadienones via Pd-catalyzed intramolecular ipso-Friedel-Crafts allylic alkylation
- Inhibitors of heat shock protein (Hsp90) as antitumor agents
- Carpanone-like molecules via an oxidative coupling/Diels-Alder cycloaddition sequence
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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