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Thermo Scientific Chemicals
Ethyl dibromoacetate, 96%
CAS: 617-33-4 | C4H6Br2O2 | 245.898 g/mol
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化學識別
CAS617-33-4
IUPAC Nameethyl 2,2-dibromoacetate
Molecular FormulaC4H6Br2O2
InChI KeyNIJGVVHCUXNSLL-UHFFFAOYSA-N
SMILESCCOC(=O)C(Br)Br
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規格
規格表
規格表Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥95.0%
Refractive Index1.4960-1.5020 @ 20?C
Ethyl dibromoacetate can be used to produce diphenoxy-acetic acid ethyl ester. It is used in organic synthesis.
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.
Applications
Ethyl dibromoacetate can be used to produce diphenoxy-acetic acid ethyl ester. It is used in organic synthesis.
Solubility
Soluble in hexane, ether, CH2Cl2, acetone, EtOAc, ethanol.
Notes
Store in cool, dry place in a well sealed container. Store away from oxidizing agents.
Ethyl dibromoacetate can be used to produce diphenoxy-acetic acid ethyl ester. It is used in organic synthesis.
Solubility
Soluble in hexane, ether, CH2Cl2, acetone, EtOAc, ethanol.
Notes
Store in cool, dry place in a well sealed container. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- José M. Concellón; Carmen Concellón and Pamela Diaz. An Efficient Synthesis of 2-Bromo-3-hydroxy Esters by Reaction of Ketones with Ethyl Dibromoacetate Promoted by Samarium Diiodide. European Journal of Organic Chemistry. 2006, 2006 (9), 2197-2200.
- José M. Concellón and Carmen Méjica. Highly Selective Synthesis of Enantiopure (S,E)-α,β-Unsaturated γ-Amino Esters Through a Sequential Reaction of Ethyl Dibromoacetate with α-Amino Aldehydes Promoted by Chromium Dichloride. European Journal of Organic Chemistry. 2007, 2007 (31), 5250-5255.