Interesting facts
Interesting Facts about Methyl 2-Chloropropanoate
Methyl 2-chloropropanoate is a fascinating organic compound that belongs to the ester family. Here are some engaging insights about this compound:
- Functional Group: Methyl 2-chloropropanoate is characterized by its ester functional group, which plays a crucial role in many biological and chemical processes.
- Synthesis: This compound can be synthesized by the reaction of methyl propanoate with thionyl chloride, helping to introduce the chlorine atom into the molecule. Such reactions are fundamental in organic synthesis, allowing the development of various derivatives.
- Reactivity: As a chlorinated ester, it exhibits interesting reactivity patterns, particularly in nucleophilic substitution reactions. This makes it a valuable intermediate in the synthesis of more complex organic compounds.
- Applications: Methyl 2-chloropropanoate has applications in the synthesis of pharmaceuticals, agrochemicals, and other chemical products. It's especially useful in the creation of compounds with specific biological activities.
- Biological Implications: Notably, esters like methyl 2-chloropropanoate can mimic naturally occurring compounds in biological systems, leading to significant implications in fragrance and flavor chemistry.
Due to its diverse applications and role in organic synthesis, understanding methyl 2-chloropropanoate opens up exciting avenues for research and innovation in the field of chemistry.
Synonyms
METHYL 2-CHLOROPROPIONATE
Methyl 2-chloropropanoate
17639-93-9
Propanoic acid, 2-chloro-, methyl ester
Propionic acid, 2-chloro-, methyl ester
Methyl alpha-chloropropionate
FDN17EXK1J
NSC-70983
DTXSID60864786
Mecpa
DTXCID10813264
2-chloropropionic acid, methyl ester
METHYL DL-ALPHA-CHLOROPROPIONATE
alpha-chloropropionic acid, methyl ester
METHYL 2-CHLOROPROPANOATE, (A+-)-
241-624-5
2-Chloropropionic acid methyl ester
(+)-Methyl (R)-2-chloropropionate
NSC 70983
MFCD00000863
Methyl .alpha.-chloropropionate
(+/-)-methyl 2-chloropropanoate
.alpha.-Chloropropionic acid methyl ester
EINECS 241-624-5
UN2933
BRN 1421535
Methyl(S)-(-)-2-Chloropropionate
(S)-(-)-Methyl 2-chloropropionate
Propanoic acid, 2-chloro-, methyl ester, (S)-
CH3CHClC(O)OCH3
methyl-2-chloropropionate
UNII-FDN17EXK1J
methyl-2-chloro-propionate
EC 241-624-5
SCHEMBL37355
4-02-00-00746 (Beilstein Handbook Reference)
SCHEMBL1269097
SCHEMBL8402377
Methyl 2-chloropropionate, 97%
2-chloropropionic acid methylester
(+/-)-Methyl 2-chloropropionate
2-Chloropropanoic acid methyl ester
NSC70983
2-chloro-propionic acid methyl ester
BBL100013
STL183303
AKOS000120934
AKOS016352933
CS-W020781
UN 2933
BS-42145
METHYL DL-.ALPHA.-CHLOROPROPIONATE
DB-015889
DB-018076
A9465
METHYL 2-CHLOROPROPANOATE, (+/-)-
NS00004721
(S)-(-)-2 Chloropropionic acid methyl ester
EN300-20536
F98166
Q27894093
F0001-0641
Methyl 2-chloropropionate [UN2933] [Flammable liquid]
Solubility of Methyl 2-chloropropanoate
Methyl 2-chloropropanoate, with the chemical formula C4H9ClO2, is an organic compound that demonstrates interesting solubility characteristics essential for various chemical applications.
When considering its solubility, we can take into account several factors:
To summarize, it can be stated that:
In essence, understanding the solubility of this compound is crucial for its effective use in chemical processes and synthesis, as well as its behavior in biological systems. As the famous saying goes, “Like dissolves like,” and this principle holds true for the interactions between methyl 2-chloropropanoate and various solvents.