869207-52-3

Usage

Chemical structure

1-Butanone, 1-[3,3,4,4,5,5-hexafluoro-2-(2-methyl-5-phenyl-3-thienyl)-1-cyclopenten-1-yl]is a complex chemical compound with a cyclopentenyl group combined with a butanone moiety.

Fluorinated compound

It contains six fluorine atoms attached to the cyclopentene ring, which may contribute to its chemical reactivity and stability.

Thienyl and phenyl groups

The presence of these groups in the molecule may influence its reactivity, stability, and potential applications.

High chemical reactivity

Due to its complex structure and the presence of multiple functional groups, 1-Butanone, 1-[3,3,4,4,5,5-hexafluoro-2-(2-methyl-5-phenyl-3-thienyl)-1-cyclopenten- 1-yl]- is likely to have high chemical reactivity.

Applications

It may have potential applications in organic synthesis and as a building block for other compounds.

Further research needed

The precise properties and potential uses of 1-Butanone, 1-[3,3,4,4,5,5-hexafluoro-2-(2-methyl-5-phenyl-3-thienyl)-1-cyclopenten- 1-yl]- would need to be determined through additional research and experimentation.

Upstream product

• 869207-50-1 C₁₆H₉F₆IS 
• 141-75-3 butyryl chloride 

Relevant academic research and scientific papers

PHOTOCHROMIC AND ELECTROCHROMIC COMPOUNDS AND SYNTHESIS AND USE THEREOF

Novel photochromic and electrochromic hexadiene compounds are described. The compounds are reversibly convertible between ring-open and ring-closed isomeric forms as indicated in structures I(o) and I(c) below. (See formula in original abstract of application) The conversion between the different isomeric forms may be induced by light or electricity. In one embodiment the compounds may include a charge transfer moiety including electron donor and acceptor groups. The electron donor and acceptor are linearly conjugated in the ring-open form to enable electron transfer but are electrically insulated in the ring-closed form. Methods for synthesizing the compounds from photochemically and/or electrically inert precursors are also described. For example, the photoresponsive compounds may be synthesized by reacting diene precursors with dienophiles in a condensation reaction. The compounds may be utilized in reactivity-gated photochromic or electrochromic applications. In one embodiment of the invention, compounds of the invention may be used in a method to selectively release a releasable agent, such as a small molecule. According to this method, a photochemically inert precursor compound is reacted with the releasable agent to form a carrier compound comprising a switching moiety, the switching moiety being reversibly convertible between a thermally unstable form and a thermally stable form. The switching moiety may be selectively converted between the first and second forms to cause controlled release of the releasable agent from the carrier compound.