Interesting facts
Interesting Facts about 2-(Methoxymethyl)oxirane
2-(Methoxymethyl)oxirane, a fascinating compound in the realm of organic chemistry, is known for its unique properties and applications. Here are some intriguing points to consider:
- Structure: This compound features a three-membered ring known as an oxirane, or epoxide, which gives it distinctive reactivity compared to other ethers. The addition of a methoxymethyl group enhances its stability and versatility.
- Reactivity: The strained ring structure of the oxirane makes it highly reactive, particularly towards nucleophiles, allowing for a variety of chemical transformations. Its ability to undergo ring-opening reactions leads to the formation of alcohols and other useful derivatives.
- Applications: 2-(Methoxymethyl)oxirane is often utilized in the synthesis of fine chemicals and pharmaceuticals. Its unique structure allows it to serve as a building block in the production of more complex molecules.
- Polymer Chemistry: This compound can be used in the preparation of polymers, particularly in the development of coatings and adhesives. Its epoxy functionality provides excellent adhesion and durability.
- Safety Considerations: As with many epoxides, 2-(Methoxymethyl)oxirane is classified as a potential irritant. Proper precautions and handling practices are essential in laboratory settings to ensure safety.
To quote a prominent chemist, "The beauty of organic chemistry lies in its complexity and the surprises that lie within the simple bonds of carbon." Indeed, 2-(Methoxymethyl)oxirane exemplifies this beauty, offering both challenges and opportunities for research and application in various fields.
Synonyms
Glycidyl methyl ether
930-37-0
Methyl glycidyl ether
Oxirane, (methoxymethyl)-
1,2-EPOXY-3-METHOXYPROPANE
Glycidol methyl ether
(Methoxymethyl)oxirane
Methylglycidyl ether
3-Methoxypropylene oxide
3-Methoxy-1,2-epoxypropane
Propane, 1,2-epoxy-3-methoxy-
2,3-Epoxypropyl-methyl ether
Oxirane, 2-(methoxymethyl)-
NSC 86950
CCRIS 2630
HSDB 5444
EINECS 213-216-7
BRN 0102505
87MK2KA66T
AI3-52869
EPIOL M
NSC-86950
DTXSID9025613
1,2-EPOXY-3-METHOXYPROPANE [HSDB]
methoxymethyloxirane
Denacol EX131
3Methoxypropylene oxide
3Methoxy1,2epoxypropane
Oxirane, (methoxymethyl)
2,3Epoxypropylmethyl ether
DENACOL EX 131
Propane, 1,2epoxy3methoxy
DTXCID205613
213-216-7
2-(Methoxymethyl)oxirane
Denacol EX-131
MFCD00005140
glycidylmethylether
28325-89-5
UNII-87MK2KA66T
2-methoxymethyl-oxirane
2-(Methoxymethyl)oxirane #
Propane,2-epoxy-3-methoxy-
LKMJVFRMDSNFRT-UHFFFAOYSA-
NSC86950
(R)-(-)-2-(Methoxymethyl)oxirane
GEO-04527
STL287735
(+/-)-GLYCIDYL METHYL ETHER
AKOS000138368
AKOS016037121
FM139095
SY053022
DB-054672
DB-054673
G0203
NS00039519
EN300-73694
F11173
Methyl glycidyl ether 1,2-Epoxy-3-methoxypropane
Q27269834
InChI=1/C4H8O2/c1-5-2-4-3-6-4/h4H,2-3H2,1H3
(S)-(+)-2-(Methoxymethyl)oxirane;(S)-(+)-Methyl glycidyl ether
Solubility of 2-(methoxymethyl)oxirane
2-(methoxymethyl)oxirane, also known as a derivative of the epoxy class, exhibits unique solubility characteristics that are influenced by its chemical structure. When discussing its solubility, several key points can be noted:
In summary, the solubility of 2-(methoxymethyl)oxirane is a complex interplay of its molecular structure and the nature of the solvent. It is essential to consider these factors to maximize its utility in chemical processes.