CAS 14594-25-3
:Pentanoic acid, 5-bromo-4-oxo-, ethyl ester
Description:
Pentanoic acid, 5-bromo-4-oxo-, ethyl ester, with the CAS number 14594-25-3, is an organic compound characterized by its ester functional group and a bromine atom substitution on the pentanoic acid backbone. This compound typically exhibits a moderate boiling point and is likely to be a colorless to pale yellow liquid at room temperature. The presence of the bromine atom introduces unique reactivity, making it useful in various chemical syntheses and applications. The ester group contributes to its solubility in organic solvents while being less soluble in water. Additionally, the keto group (4-oxo) enhances its reactivity, potentially allowing for further chemical transformations. As with many organic compounds, it is essential to handle this substance with care, observing appropriate safety protocols due to its potential toxicity and reactivity. Overall, pentanoic acid, 5-bromo-4-oxo-, ethyl ester is a valuable compound in organic chemistry, particularly in the synthesis of more complex molecules.
Formula:C7H11BrO3
InChI:InChI=1S/C7H11BrO3/c1-2-11-7(10)4-3-6(9)5-8/h2-5H2,1H3
InChI key:InChIKey=HZTCCISWRZQSRU-UHFFFAOYSA-N
SMILES:C(CC(CBr)=O)C(OCC)=O
Synonyms:- 5-Bromo-4-oxo-pentanoic acid ethyl ester
- Pentanoic acid, 5-bromo-4-oxo-, ethyl ester
- Levulinic acid, 5-bromo-, ethyl ester
- Ethyl 5-bromo-4-oxopentanoate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Ethyl 5-Bromo-4-Oxopentanoate
CAS:Controlled ProductFormula:C7H11BrO3Color and Shape:NeatMolecular weight:223.064


