Interesting facts
Interesting Facts About Ethyl 2-(4-chloro-2-methyl-phenoxy)acetate
Ethyl 2-(4-chloro-2-methyl-phenoxy)acetate, often recognized for its applications in organic synthesis and as an important intermediate in various chemical reactions, holds several intriguing characteristics that provide insight into its utility and significance in the field of chemistry. Here are some noteworthy aspects:
- Chemical Structure: This compound features a unique arrangement that includes an ethyl group, a chloro substituent, and a phenoxy group, which contribute to its versatile reactivity. The presence of the Cl atom enhances its electrophilic properties, making it useful in nucleophilic substitution reactions.
- Synthesis: Ethyl 2-(4-chloro-2-methyl-phenoxy)acetate is typically synthesized via the reaction of 4-chloro-2-methylphenol with ethyl chloroacetate in the presence of a base. This method exemplifies the utility of phenolic compounds in organic synthesis.
- Applications: This compound serves as a precursor in the formation of various biologically active molecules, particularly in the pharmaceutical and agrochemical industries. Its derivatives are often explored for herbicidal and fungicidal activities.
- Biological Relevance: Due to its structural features, ethyl 2-(4-chloro-2-methyl-phenoxy)acetate may exhibit interesting biological activities, potentially influencing enzyme systems or affecting plant growth.
- Future Research: Ongoing studies aim to explore new pathways for the synthesis of this compound and its potential derivatives, thereby expanding the existing knowledge regarding its chemical reactivity and biological significance.
As a student or an aspiring chemist, understanding compounds like ethyl 2-(4-chloro-2-methyl-phenoxy)acetate not only enriches your knowledge but also enhances your ability to engage in practical applications in both research and industry. Keep exploring the fascinating world of organic compounds!
Synonyms
MCPA-ethyl
MCPA ethyl ester
2698-38-6
Mcpee
MCPA-ethyl [ISO]
Ethyl 2-methyl-4-chlorophenoxyacetate
4-Chloro-2-methylphenoxyacetic acid ethyl ester
Acetic acid, (4-chloro-2-methylphenoxy)-, ethyl ester
UNII-KUS1I4G36I
EINECS 220-275-2
KUS1I4G36I
4-Chloro-2-methylphenoxyacetic acid ethylester
NSC 409764
4-Chloro-2-methylphenoxyacetic acid, ethyl ester
ACETIC ACID, ((4-CHLORO-o-TOLYL)OXY)-, ETHYL ESTER
BRN 2117137
AI3-16669
4-Chloro-2-methylphenoxy acetic acid ethyl ester
NSC-409764
DTXSID60181480
4-06-00-01991 (Beilstein Handbook Reference)
ACETIC ACID, 2-(4-CHLORO-2-METHYLPHENOXY)-, ETHYL ESTER
MCPAEE
DTXCID70103971
Acetic acid, (4-chloro-2-methylphenoxy)-, ethyl ester (9CI)
220-275-2
ouydekfrlsfdmu-uhfffaoysa-n
Mcpa-ethyl ester
ethyl 2-(4-chloro-2-methylphenoxy)acetate
Ethyl 4-chloro-o-tolyloxyacetate
WLN: GR C1 DO1VO2
SCHEMBL5416139
NSC409764
STK028425
AKOS003658306
Ethyl (4-chloro-2-methylphenoxy)acetate
1ST22048
DB-047097
Ethyl (4-chloro-2-methylphenoxy)acetate #
CS-0361405
NS00028240
2-(4-Chloro-2-methylphenoxy)acetic acid ethyl ester
Q27282451
Solubility of Ethyl 2-(4-chloro-2-methyl-phenoxy)acetate
Ethyl 2-(4-chloro-2-methyl-phenoxy)acetate is an organic compound that exhibits specific solubility characteristics due to its molecular structure. Understanding its solubility is crucial for applications in chemical synthesis and formulation. Here's a breakdown of its solubility properties:
Overall, the solubility of ethyl 2-(4-chloro-2-methyl-phenoxy)acetate illustrates a common trend among similar compounds, where non-polar characteristics limit solubility in polar solvents like water, making organic solvents the preferred medium for dissolution. Understanding these principles is vital for effective usage in practical applications.