
CAS 3674-13-3: Ethyl 2,3-dibromopropanoate
Formula:C5H8Br2O2
InChI:InChI=1S/C5H8Br2O2/c1-2-9-5(8)4(7)3-6/h4H,2-3H2,1H3
InChI key:InChIKey=OENICUBCLXKLJQ-UHFFFAOYSA-N
SMILES:C(C(CBr)Br)(OCC)=O
Synonyms:- 2,3-Dibromopropanoic acid ethyl ester
- 2,3-Dibromopropionic acid ethyl ester
- Ethyl 2,3-Dibromopropanoate
- Ethyl α,β-dibromopropionate
- NSC 60552
- Propanoic acid, 2,3-dibromo-, ethyl ester
- Propionic acid, 2,3-dibromo-, ethyl ester
- ethyl (2R)-2,3-dibromopropanoate
- ethyl (2S)-2,3-dibromopropanoate
- Ethyl 2,3-dibromopropionate
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Found 9 products.
Ethyl 2,3-Dibromopropionate
CAS:Purity:97.0%Color and Shape:LiquidMolecular weight:259.92498779296875Ethyl 2,3-dibromopropionate, 97%
CAS:Ethyl 2,3-dibromopropionate is used as pharmaceutical Intermediates. It is a building block that has been used as a catalyst for the polymerization of ethyl acrylate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C5H8Br2O2Purity:97%Color and Shape:Liquid, Clear colorless to pale yellowMolecular weight:259.93Ethyl 2,3-Dibromopropanoate
CAS:Controlled ProductApplications Ethyl 2,3-Dibromopropanoate is a building block that has been used as a catalyst for the polymerization of ethyl acrylate. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Sakota, N., et. al.: Kogyo Kagaku Zasshi, 72, 975 (1969)Formula:C5H8Br2O2Color and Shape:NeatMolecular weight:259.92Ethyl 2,3-Dibromopropionate
CAS:Formula:C5H8Br2O2Purity:98%Color and Shape:LiquidMolecular weight:259.9238Ethyl 2,3-Dibromopropionate
CAS:Formula:C5H8Br2O2Purity:>98.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:259.93Ethyl 2,3-dibromopropionate
CAS:Ethyl 2,3-dibromopropionate is a synthetic compound that is used in the preparation of other chemicals. It has been shown to have potent antiplatelet activity and inhibitory effect on platelet aggregation. Ethyl 2,3-dibromopropionate can be synthesized by the reaction of benzodioxan with hydrogen chloride in the presence of quinoline derivatives. The synthesis is asymmetric and yields two enantiomers: (2S)-ethyl 2,3-dibromopropionate and (2R)-ethyl 2,3-dibromopropionate.Formula:C5H8Br2O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:259.92 g/molRef: 3D-FE179028
Discontinued product