[A10448] CAS 105-36-2 | Ethyl bromoacetate, 98% | Alfa
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Brand: Alfa Aesar
105-36-2 | C4H7BrO2 | ethyl bromoacetate
Chemical Identifiers
CAS
105-36-2
Molecular Weight (g/mol)
167.00
Synonym
ethyl bromoacetate
SMILES
CCOC(=O)CBr
InChI Key
PQJJJMRNHATNKG-UHFFFAOYSA-N
Molecular Formula
C4H7BrO2
IUPAC Name
ethyl 2-bromoacetate
Specifications
Appearance (Color)
Clear colorless
Refractive Index
1.4495-1.4535 @ 20?C
Assay (GC)
≥97.5%
Form
Liquid
Identification (FTIR)
Conforms
설명
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.
Applications
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.
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.
Solubility
Miscible with ethanol, acetone, benzene and ethyl ether. Immiscible with water.
Notes
It is a lachrymator. Incompatible with strong oxidizing agents.
Other References:
UN Number:UN1603
GHS Hazard and Precautionary Statements
Hazard Statements:H226-H300+H310+H330
GHS H StatementH300-H310-H330-H226 Fatal if swallowed. Fatal in contact with skin. Fatal if inhaled. Flammable liquid and vapor.
Precautionary Statements: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
Risk & Safety
TSCA:YesRTECS Number:AF6000000
경고:RUO – Research Use Only
CAS105-36-2FORMULAC4H7BrO2HAZARD CLASS6.1EINECS203-290-9MDLMFCD00000191PACKAGING GROUPII
| Pakage | 100g, 2500g, 500g |
|---|---|
| brand | Alfa Aesar |
