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About This Item
Linear Formula:
BrC6H4COCH2CO2C2H5
CAS Number:
Molecular Weight:
271.11
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥95.0%
refractive index
n20/D 1.5700 (lit.)
bp
268-269 °C (lit.)
density
1.432 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)CC(=O)c1ccc(Br)cc1
InChI
1S/C11H11BrO3/c1-2-15-11(14)7-10(13)8-3-5-9(12)6-4-8/h3-6H,2,7H2,1H3
InChI key
PBDYXCKRDRCJDC-UHFFFAOYSA-N
General description
Ethyl (4-bromobenzoyl)acetate can be prepared by employing the following reagents:
- ethyl acetylacetate
- petroleum ether
- NaOH
- 4-bromobenzoyl chloride
Application
Ethyl (4-bromobenzoyl)acetate may be used to synthesize 2-(carboethoxy)-3-(4′-bromo)phenylquinoxaline 1,4-dioxide.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Syntheses and eletroluminescence properties of red emitting copolymers with different lengths of diketopyrrolopyrrole units.
Xu Y, et al.
Synthetic Metals, 160(19), 2135-2142 (2010)
Comparative Use of Solvent-free KF-Al2O3 and K2CO3 in Acetone in the Synthesis of Quinoxaline 1, 4-Dioxide Derivatives Designed as Antimalarial Drug Candidates.
Lima LM, et al.
Journal of Heterocyclic Chemistry, 42(7), 1381-1385 (2005)
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