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799-34-8 | 2-(2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptoxymethyl)oxirane

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2-(2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptoxymethyl)oxirane, also known as perfluoromethyl epoxide, is a fluorinated organic compound with a unique structure that makes it useful in scientific research...

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CAS:799-34-8 | 2-(2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptoxymethyl)oxirane ,Description

2-(2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptoxymethyl)oxirane, also known as perfluoromethyl epoxide, is a fluorinated organic compound with a unique structure that makes it useful in scientific research. 
 

Scientific Research Applications

 

Polymer Synthesis and Properties

2-(2,2,3,3,4,4,5,5,6,6,7,7-Dodecafluoroheptoxymethyl)oxirane is involved in the synthesis of specialized polymers. For instance, its derivatives have been used in the synthesis of polyoxiranes, displaying unique properties due to their fluorinated structures. These polymers exhibit significant potential in various applications due to their molecular weight and structural characteristics (Li, 2012) .

Ring-Opening Polymerization

The compound plays a crucial role in ring-opening polymerization processes. This technique is fundamental in creating polymers with specific structural features. The process involves the use of initiators like boron trifluoride etherate, highlighting the versatility of this compound in polymer chemistry (Shih et al., 1982).

Catalytic Hydrogenation Studies

Research on catalytic hydrogenation of oxiranes, including derivatives of the studied compound, provides insights into chemical reaction mechanisms and potential industrial applications. These studies offer valuable information on the behavior of these compounds under various chemical conditions (Kuevi et al., 2012).

Chemical Ionization and Analytical Chemistry

Oxirane derivatives, including the mentioned compound, are significant in chemical ionization processes. Their unique reactivity profiles make them suitable for analyzing different classes of compounds in mass spectrometry, enhancing selectivity and discrimination in analytical chemistry (Lange, 1993).

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