CAS 32803-73-9
:Benzenepropanoic acid, b-chloro-a-oxo-, methyl ester
Description:
Benzenepropanoic acid, b-chloro-a-oxo-, methyl ester, identified by its CAS number 32803-73-9, is an organic compound characterized by its ester functional group and the presence of a chloro substituent. This compound features a benzene ring attached to a propanoic acid moiety, which is further modified by a b-chloro and a keto group. The methyl ester form indicates that the carboxylic acid group has been esterified with methanol. This compound is likely to exhibit moderate polarity due to the presence of both the ester and the chloro groups, influencing its solubility in organic solvents. It may also demonstrate reactivity typical of esters, such as hydrolysis under acidic or basic conditions. Additionally, the presence of the chloro group can impart unique chemical properties, potentially affecting its reactivity and interactions with biological systems. Overall, this compound may find applications in organic synthesis, pharmaceuticals, or as an intermediate in chemical manufacturing, although specific applications would depend on further research and characterization.
Formula:C10H9ClO3
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
Methyl 3-chloro-2-oxo-3-phenylpropanoate
CAS:<p>Methyl 3-chloro-2-oxo-3-phenylpropanoate is a covalent analog of paclitaxel. It has been synthesized by the chemoenzymatic reaction of acetyl chloride, chloroacetic acid, and phenylacetaldehyde in the presence of thiosemicarbazide. The yield is 80%. The product has been shown to have similar biological activity as paclitaxel. The synthesis of methyl 3-chloro-2-oxo-3-phenylpropanoate is based on nature.</p>Formula:C10H9ClO3Purity:Min. 95%Molecular weight:212.63 g/mol
