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About This Item
Linear Formula:
(C6H5)3P(I)C2H5
CAS Number:
Molecular Weight:
418.25
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
EC Number:
225-245-2
Beilstein/REAXYS Number:
3659323
MDL number:
Assay:
95%
Form:
powder
Quality Level
assay
95%
form
powder
reaction suitability
core: phosphonium, reaction type: C-C Bond Formation
mp
164-168 °C (lit.)
functional group
phosphine
SMILES string
[I-].CC[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C20H20P.HI/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;/h3-17H,2H2,1H3;1H/q+1;/p-1
InChI key
SLAFUPJSGFVWPP-UHFFFAOYSA-M
Application
Ethyltriphenylphosphonium iodide can be used as:
- An efficient catalyst for N,N-dimethylation of primary aromatic amines with methyl alkyl carbonates.
- A phase transfer catalyst for the synthesis of 3-hydroxyflavones from chalcones via Algar−Flynn−Oyamada synthesis.
Reactant involved in:
- Synthesis of diarylmethine derivatives, phosphonium salts, and bismuth(III) polynuclear halide complexes
- Asymmetric hydrogenation
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
监管及禁止进口产品
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Find documentation for the products that you have recently purchased in the Document Library.
Phase Transfer Catalysis Extends The Scope of The Algar-Flynn-Oyamada Synthesis of 3-Hydroxyflavones
Nhu D, et al.
Australian Journal of Chemistry, 68(7), 1102-1107 (2015)
Selective N, N-dimethylation of primary aromatic amines with methyl alkyl carbonates in the presence of phosphonium salts
Selva M, et al.
The Journal of Organic Chemistry, 71(15), 5770-5773 (2006)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 389471-100G | 04061833547298 |
