Interesting facts
Interesting Facts About Methyl 2-Chloro-3-(4-chlorophenyl)propanoate
Methyl 2-chloro-3-(4-chlorophenyl)propanoate is a fascinating compound that belongs to the family of chloroesters. This compound exhibits several properties that make it worthy of study in various fields, particularly in organic chemistry and medicinal chemistry. Here are some intriguing aspects of this compound:
- Structural Diversity: The molecular structure of this compound is particularly interesting due to the presence of both a chlorine atom and a phenyl group. This diversity in structure often leads to unique reactivity that chemists find valuable in synthetic applications.
- Synthetic Applications: Due to its reactivity, methyl 2-chloro-3-(4-chlorophenyl)propanoate can serve as a useful intermediate in the synthesis of more complex molecules. It is often employed in the creation of pharmaceuticals and agrochemicals.
- Bioactivity Exploration: The chlorinated phenyl moiety in this compound could contribute to noteworthy biological activities. Compounds with similar structures have been researched for their potential anti-inflammatory and anticancer properties.
- Environmental Considerations: As with many chlorinated compounds, there is ongoing research into the environmental impact and degradation pathways of methyl 2-chloro-3-(4-chlorophenyl)propanoate. Understanding its behavior in natural settings is crucial for assessing safety and ecological risks.
- Regulatory Attention: Given its chemical nature, this compound might draw interest from regulatory bodies focused on chemical safety and public health. Research into its effects and safe handling practices is essential.
In summary, methyl 2-chloro-3-(4-chlorophenyl)propanoate is more than just a chemical formula; it represents a point of intersection in various fields, from synthesis and pharmaceuticals to environmental impact assessments. As scientific research continues, this compound may reveal even more of its secrets, challenging chemists to explore its potential and applications.
Synonyms
Chlorfenprop-methyl
14437-17-3
Methachlorphenprop
Chlorphenprop-methyl
Chlorfenpropmethyl
Methyl 2-chloro-3-(4-chlorophenyl)propionate
Benzenepropanoic acid, alpha,4-dichloro-, methyl ester
894064M9QG
DTXSID5041770
Methyl-2-chloro-3-(4-chlorophenyl)propionate
BAY-70533
B-57-10
DTXCID3021770
238-413-5
Bidisin
Chlorophenprop-methyl
Chlorofenprop-methyl
Bayer 70533
Methyl 2-chloro-3-(4-chlorophenyl)propanoate
BAY 70533
2-Chloro-3-(4-chlorophenyl)propionic acid methyl ester
W5769
2-Chloro-3-(4-chlorophenyl)-methylpropionate
Methyl 2-chloro-3-(p-chlorophenyl)propionate
3-(4-Chlorphenyl)-2-chlorpropionsaeuremethylester
Methylester kyseliny 2-chlor-3-p-chlorfenylpropionove
Benzenepropanoic acid, .alpha.,4-dichloro-, methyl ester
Propionic acid, 2-chloro-3-(4-chlorophenyl)-, methyl ester
Caswell No. 557A
Chlorfenprop-methyl [BSI:ISO]
EINECS 238-413-5
Methyl alpha-p-dichlorohydrocinnamate
EPA Pesticide Chemical Code 557200
Methyl alpha,4-dichlorophenylpropanoate
BRN 2331933
UNII-894064M9QG
3-(4-Chlorphenyl)-2-chlorpropionsaeuremethylester [German]
Methylester kyseliny 2-chlor-3-p-chlorfenylpropionove [Czech]
SCHEMBL163965
Hydrocinnamic acid, p,.alpha.-dichloro-, methyl ester
orb1986271
CHEBI:82236
CHLORFENPROP-METHYL [ISO]
AKOS017415075
Methyl .alpha.,4-dichlorophenylpropanoate
NS00021661
Methyl 3-(4-chlorophenyl)-2-chloropropionate
C19115
Methyl 2-chloro-3-(4-chlorophenyl)propanoate #
B 57-10
Q27155829
Chlorofenprop-methyl, PESTANAL(R), analytical standard
Methyl .alpha.-chloro-.beta.-(p-chlorophenyl)propionate
Solubility of Methyl 2-chloro-3-(4-chlorophenyl)propanoate
The solubility of methyl 2-chloro-3-(4-chlorophenyl)propanoate can be influenced by several factors, primarily due to its molecular structure and the presence of chlorinated groups. Understanding its solubility behavior is essential for applications in both laboratory and industrial settings. Here are the key characteristics:
In summary, while methyl 2-chloro-3-(4-chlorophenyl)propanoate may see good solubility in various organic solvents, its solubility in water is restricted. As a rule of thumb, “like dissolves like” is a fundamental principle in chemistry that can guide expectations regarding this compound’s solubility behaviors across different media.