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About This Item
Linear Formula:
(C6H5)3PBr2
CAS Number:
Molecular Weight:
422.09
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-855-1
Beilstein/REAXYS Number:
917652
MDL number:
Assay:
96%
Form:
solid
Quality Level
assay
96%
form
solid
mp
235 °C (dec.) (lit.)
functional group
phosphine
SMILES string
BrP(Br)(c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C18H15Br2P/c19-21(20,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI key
OCXGTPDKNBIOTF-UHFFFAOYSA-N
Application
Reagent used in the preparation of alkyl and aryl bromides from alcohols and phenols without rearrangement.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Y Satoh et al.
Journal of medicinal chemistry, 36(23), 3580-3594 (1993-11-12)
A series of chromene derivatives was synthesized and evaluated for their in vitro and ex vivo 5-lipoxygenase (5-LO) inhibitory activity. These compounds were prepared by condensation of appropriate salicyl aldehydes with alpha, beta-unsaturated carbonyl compounds, followed by transformation to the
Synthetic Communications, 22, 2945-2945 (1992)
Journal of the American Chemical Society, 86, 964-964 (1964)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 270946-25G | 04061826143346 |
| 270946-5G | 04061826143353 |
