| Weight | 210.984 g/mol |
|---|---|
| Formula | C6H5Cl2O2P |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
PHENYL DICHLOROPHOSPHATE (770-12-7)
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- Direct transformation of carboxylic acids to thiol esters induced by phenyl dichlorophosphate (Canadian Journal of Chemistry, 1980)
- Syntheses of -lactams from acetic acids and imines induced by phenyl dichlorophosphate reagent (Tetrahedron, 1985)
- Reagents and Synthetic Methods 25. A New Method for the Synthesis of Acyl Azides from Carboxylic Acids and Sodium Azide Induced by Phenyl Dichlorophosphate (Synthetic Communications, 1983)
- Phenyl dichlorophosphate as an activating agent in the pfitzner-moffatt oxidation (Tetrahedron Letters, 1988)
- Facile fragmentation of pinenes using dimethyl sulfoxide activated by phenyl dichlorophosphate or phosphorus oxychloride. Efficient conversion of -pinene to carvone (Tetrahedron Letters, 1989)
- Reagents and Synthetic Methods 17. Phenyl-Dichlorophosphate-Dimethylformamide Complex. Direct High Yield Annelation of Imines to Alpha-Phtalimido Beta-Lactams (Synthetic Communications, 1982)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)OP(=O)(Cl)Cl
-
InChIKeyTXFOLHZMICYNRM-UHFFFAOYSA-N
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