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About This Item
Linear Formula:
BrC6H4COCH2CO2C2H5
CAS Number:
Molecular Weight:
271.11
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
assay
≥95%
refractive index
n20/D 1.5545 (lit.)
density
1.417 g/mL at 25 °C (lit.)
functional group
bromo
ester
ketone
SMILES string
CCOC(=O)CC(=O)c1ccccc1Br
InChI
1S/C11H11BrO3/c1-2-15-11(14)7-10(13)8-5-3-4-6-9(8)12/h3-6H,2,7H2,1H3
InChI key
IFSMFGOJDWUHEW-UHFFFAOYSA-N
General description
Ethyl (2-bromobenzoyl)acetate [Ethyl 3-(2-bromophenyl)-3-oxopropanoate] can be synthesized from the condensation reaction between an aldehyde and ethyl diacetate in the presence of zeolite Hβ (catalyst).[1]
application
Reactant for preparation of:
- Cambinol analogs as sirtuin inhibitors with antitumor action
- Quinolones and indoles by cyclodehydration
- N-allyl/propargyl enamine carboxylates
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Simple and high yielding syntheses of ?-ketoesters catalyzed by zeolites.
Balaji BS and Chanda BM.
Tetrahedron, 54, 13237-13252 (1998)
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