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Ethyl bromoacetate, 98%, Thermo Scientific Chemicals
$66.56 - $702.27
Chemical Identifiers
CAS | 105-36-2 |
---|---|
Molecular Formula | C4H7BrO2 |
Molecular Weight (g/mol) | 167.002 |
MDL Number | MFCD00000191 |
InChI Key | PQJJJMRNHATNKG-UHFFFAOYSA-N |
Synonym | ethyl bromoacetate, antol, ethyl bromacetate, bromoacetic acid ethyl ester, ethyl monobromoacetate, acetic acid, bromo-, ethyl ester, ethoxycarbonylmethyl bromide, bromoacetic acid, ethyl ester, ethyl alpha-bromoacetate, ethyl bromo acetate |
PubChem CID | 7748 |
IUPAC Name | ethyl 2-bromoacetate |
SMILES | CCOC(=O)CBr |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAA1044822
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Thermo Scientific Chemicals
A1044822 |
100 g |
Each for $66.56
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AAA1044836
|
Thermo Scientific Chemicals
A1044836 |
500 g |
Each for $207.99
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AAA104480E
|
Thermo Scientific Chemicals
A104480E |
2500 g |
Each for $702.27
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Description
Ethyl bromoacetate is widely used as an alkylating reagent involved in the Reformatsky reaction to prepare the beta-hydroxy esters by reacting with carbonyl compounds. It is also used for the syntheses of witting reagent, artificial diethylstilbestrol antigen, 3-phenyl-1-naphthol and steroidal thiazolidinone derivatives. It finds applications in the preparation of reversibly photoresponsive coumarin-stabilized polymeric nanoparticles in an aqueous medium which act as a detectable drug carrier.
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.
ApplicationsEthyl bromoacetate is widely used as an alkylating reagent involved in the Reformatsky reaction to prepare the beta-hydroxy esters by reacting with carbonyl compounds. It is also used for the syntheses of witting reagent, artificial diethylstilbestrol antigen, 3-phenyl-1-naphthol and steroidal thiazolidinone derivatives. It finds applications in the preparation of reversibly photoresponsive coumarin-stabilized polymeric nanoparticles in an aqueous medium which act as a detectable drug carrier.
Solubility
Miscible with ethanol, acetone, benzene and ethyl ether. Immiscible with water.
Notes
It is a lachrymator. Incompatible with strong oxidizing agents.
Chemical Identifiers
105-36-2 | |
167.002 | |
PQJJJMRNHATNKG-UHFFFAOYSA-N | |
7748 | |
CCOC(=O)CBr |
C4H7BrO2 | |
MFCD00000191 | |
ethyl bromoacetate, antol, ethyl bromacetate, bromoacetic acid ethyl ester, ethyl monobromoacetate, acetic acid, bromo-, ethyl ester, ethoxycarbonylmethyl bromide, bromoacetic acid, ethyl ester, ethyl alpha-bromoacetate, ethyl bromo acetate | |
ethyl 2-bromoacetate |
Specifications
105-36-2 | |
1.506 g/mL | |
47°C (117°F) | |
C4H7BrO2 | |
BrCH2CO2CH2CH3 | |
100 g | |
ethyl bromoacetate, antol, ethyl bromacetate, bromoacetic acid ethyl ester, ethyl monobromoacetate, acetic acid, bromo-, ethyl ester, ethoxycarbonylmethyl bromide, bromoacetic acid, ethyl ester, ethyl alpha-bromoacetate, ethyl bromo acetate | |
PQJJJMRNHATNKG-UHFFFAOYSA-N | |
ethyl 2-bromoacetate | |
7748 | |
98% |
°C to 38°C | |
159°C | |
98% | |
1.451 | |
MFCD00000191 | |
UN1603 | |
Miscible with ethanol,acetone,benzene and ethyl ether. Immiscible with water. | |
CCOC(=O)CBr | |
167.002 | |
167 | |
Ethyl bromoacetate |
Safety and Handling
GHS H Statement
H300-H310-H330-H226
Fatal if swallowed.
Fatal in contact with skin.
Fatal if inhaled.
Flammable liquid and vapor.
P210-P233-P235-P240-P241-P242-P243-P260-P262-P264b-P270-P271-P280-P284-P301+P310-P303+P361+P353-P304+P340-P310-P330-P363-P370+P378q-P501c
H226-H300+H310+H330
DOTInformation : Transport Hazard Class: 6.1; Packing Group: II; Proper Shipping Name: ETHYL BROMOACETATE
EINECSNumber : 203-290-9
RTECSNumber : AF6000000
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only