| Weight | 202.982 g/mol |
|---|---|
| Formula | C4H5BrF2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Ethyl bromodifluoroacetate (667-27-6)
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- Visible-Light-Mediated Radical Aryldifluoroacetylation of Alkynes with Ethyl Bromodifluoroacetate for the Synthesis of 3-Difluoroacetylated Coumarins (Journal of Organic Chemistry, 2015)
- Enantioselective Synthesis of ,-Difluoro--amino Acid and 3,3-Difluoroazetidin-2-one via the Reformatsky-Type Reaction of Ethyl Bromodifluoroacetate with Chiral 1,3-Oxazolidines (Journal of Organic Chemistry, 1999)
- Reactions of ethyl bromodifluoroacetate in the presence of copper powder (Journal of Fluorine Chemistry, 2004)
- Direct Introduction of Ethoxycarbonyldifluoromethyl-Group to Heteroarenes with Ethyl Bromodifluoroacetate via Visible-Light Photocatalysis (Chinese Journal of Chemistry, 2013)
- Convenient asymmetric synthesis of beta-substituted alpha,alpha-difluoro-beta-amino acids via Reformatsky reaction between Davis' N-sulfinylimines and ethyl bromodifluoroacetate. (Journal of Organic Chemistry, 2003)
- Rhodium-catalyzed Reformatsky-type reaction of ethyl bromodifluoroacetate (Tetrahedron Letters, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)C(F)(F)Br
-
InChIKeyIRSJDVYTJUCXRV-UHFFFAOYSA-N
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Synthesis
Reactant
+
Chloroethane
(Ester from carboxilic acid(SN2))
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Ethyl bromodifluoroacetate
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