02615
(Ethoxycarbonylmethyl)triphenylphosphonium chloride
technical, ≥90% (AT)
Synonym(s):
(2-Ethoxy-2-oxoethyl)triphenylphosphonium chloride
About This Item
Recommended Products
grade
technical
Assay
≥90% (AT)
reaction suitability
reaction type: C-C Bond Formation
mp
120-123 °C (dec.)
120-123 °C (lit.)
functional group
ester
phosphine
storage temp.
2-8°C
SMILES string
[Cl-].CCOC(=O)C[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C22H22O2P.ClH/c1-2-24-22(23)18-25(19-12-6-3-7-13-19,20-14-8-4-9-15-20)21-16-10-5-11-17-21;/h3-17H,2,18H2,1H3;1H/q+1;/p-1
InChI key
DJGHVEPNEJKZBF-UHFFFAOYSA-M
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Application
- Preparation of disubstituted tetrahydrofurans as selective serotonin re-uptake inhibitors for the treatment of depression
- Ring-opening reactions with Wittig reagents
- Enantioselective total synthesis of the phytotoxic lactone herbarumin III via Keck′s asymmetric allylation and Sharpless epoxidation
- Synthesis of fluorobenzofurans via microwave-assisted tandem intramolecular Wittig and Claisen rearrangement reactions
- Preparation of phosphonium derivatives of coumarin
Other Notes
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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