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Names | |
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IUPAC name
Ethyl 2-bromo-2,2-difluoroacetate
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Systematic IUPAC name
Ethyl 2,2-dibromo-2-fluoro-acetate | |
Other names
Difluorobromoacetic acid ethyl ester
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Identifiers | |
3D model (
JSmol)
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ChemSpider | |
ECHA InfoCard | 100.010.517 |
EC Number |
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PubChem
CID
|
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UNII | |
CompTox Dashboard (
EPA)
|
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Properties | |
F2BrCHCO2CH2CH3 | |
Molar mass | 202.983 g·mol−1 |
Appearance | Colorless to slightly yellow liquid |
Density | 1.583 g/mL |
Boiling point | 82 °C (180 °F; 355 K) pressure is at 33 torr |
Vapor pressure | 1.36 mmHg at 25°C |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Danger | |
H225, H314 | |
P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Ethyl bromodifluoroacetate is an ester with the chemical formula F2 Br C H−C O2CH2CH3. It can be used to introduce the CF2 group when synthesising chemical compounds. It is a colorless to yellow liquid. It is an ethyl ester of bromodifluoroacetic acid.
Ethyl fluorosulfonoxydifluoroacetate can react with sodium bromide (NaBr) to produce ethyl bromodifluoroacetate. And this reaction could happen in the solvent sulfolane. The reactions takes 12 hours at 100 °C with a yield of 31%.
Ethyl bromodifluoroacetate, and other similar compounds containing a CF2 units can be generated using the Reformatsky reagent with aldehydes and ketones. This yields 2,2-difluoro-3-hydroxy esters. Also ethyl bromdifluoroacetate is considered to be a good compound in generation of compounds and for testing with other organic compounds like lactones, imines and other amino acids. [2]
![]() | |
Names | |
---|---|
IUPAC name
Ethyl 2-bromo-2,2-difluoroacetate
| |
Systematic IUPAC name
Ethyl 2,2-dibromo-2-fluoro-acetate | |
Other names
Difluorobromoacetic acid ethyl ester
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.010.517 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
F2BrCHCO2CH2CH3 | |
Molar mass | 202.983 g·mol−1 |
Appearance | Colorless to slightly yellow liquid |
Density | 1.583 g/mL |
Boiling point | 82 °C (180 °F; 355 K) pressure is at 33 torr |
Vapor pressure | 1.36 mmHg at 25°C |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Danger | |
H225, H314 | |
P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Ethyl bromodifluoroacetate is an ester with the chemical formula F2 Br C H−C O2CH2CH3. It can be used to introduce the CF2 group when synthesising chemical compounds. It is a colorless to yellow liquid. It is an ethyl ester of bromodifluoroacetic acid.
Ethyl fluorosulfonoxydifluoroacetate can react with sodium bromide (NaBr) to produce ethyl bromodifluoroacetate. And this reaction could happen in the solvent sulfolane. The reactions takes 12 hours at 100 °C with a yield of 31%.
Ethyl bromodifluoroacetate, and other similar compounds containing a CF2 units can be generated using the Reformatsky reagent with aldehydes and ketones. This yields 2,2-difluoro-3-hydroxy esters. Also ethyl bromdifluoroacetate is considered to be a good compound in generation of compounds and for testing with other organic compounds like lactones, imines and other amino acids. [2]