Interesting facts
Interesting Facts about Methyl 2,2-Dichloroacetate
Methyl 2,2-dichloroacetate is a fascinating compound that belongs to the family of esters, which are widely utilized in both industrial and laboratory settings. Here are some captivating aspects that highlight its significance:
- Synthesis: This compound is primarily synthesized through the esterification of 2,2-dichloroacetic acid with methanol. This reaction showcases the beautiful interplay between organic reactants, yielding an important chemical useful in various applications.
- Applications: Methyl 2,2-dichloroacetate is particularly valued in organic synthesis. It serves as an alkylating agent in reactions to create more complex molecules, which are essential in pharmaceuticals and agrochemical development.
- Regulatory Attention: Due to its dichloro component, this compound is subject to regulatory scrutiny. Understanding its ecological and health impacts is crucial, making it a topic of interest in environmental chemistry.
- Reactivity: The presence of the dichloro substituents enhances the compound's reactivity, opening doors for further chemical transformations. Chemists often explore its potential in synthesizing various derivatives by modifying its functional groups.
- Research Opportunities: Methyl 2,2-dichloroacetate is often used in research settings to study reaction mechanisms and the behavior of esters under different conditions. As a student, delving into such compounds can broaden your understanding of organic reactions.
As you study this compound, remember the words of renowned chemist Linus Pauling: "The best way to have a good idea is to have lots of ideas." Exploring the properties and potential of methyl 2,2-dichloroacetate can lead to innovative applications and further learning in the field of chemistry!
Synonyms
METHYL DICHLOROACETATE
116-54-1
Dichloroacetic acid methyl ester
Methyl 2,2-dichloroacetate
Acetic acid, dichloro-, methyl ester
Acetic acid, 2,2-dichloro-, methyl ester
CCRIS 7740
NSC 2882
EINECS 204-146-8
HG7W497BZU
UN2299
AI3-18187
NSC-2882
DTXSID2059433
UN 2299
ACETIC ACID,DICHLORO,METHYL ESTER
methyl dichloroethanoate
Dicloroacetato de metilo
Dichloracetate de methyle
WLN: GYGVO1
Methyl 2,2dichloroacetate
METHYLDICHLOROACETATE
UNII-HG7W497BZU
SCHEMBL270012
Dichloroacetic acid-methyl ester
DTXCID6033372
NSC2882
AAA11654
Acetic acid, dichloro, methyl ester
MFCD00000843
STL281852
1,1-Dichloro-2-methoxy-2-oxoethane
AKOS009028820
Acetic acid, 2,2dichloro, methyl ester
Dichloracetate de methyle (French DOT)
Dicloroacetato de metilo (Spanish DOT)
DICHLOROACETIC ACID, METHYL ESTER
D0309
Methyl dichloroacetate [UN2299] [Poison]
NS00020932
EN300-19203
E78802
Q63408678
F1908-0134
Methyl dichloroacetate, PESTANAL(R), analytical standard
Dichloroacetic acid-methyl ester 1000 microg/mL in Methyl-tert-butyl ether
204-146-8
Solubility of Methyl 2,2-Dichloroacetate
Methyl 2,2-dichloroacetate, with the chemical formula C4H6Cl2O2, exhibits interesting solubility characteristics that are influenced by its molecular structure. Here are some key points regarding its solubility:
In summary, the solubility of methyl 2,2-dichloroacetate is primarily governed by its polar nature and ability to interact effectively with polar solvents, which enhances its utility in various chemical applications.