(11bS)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]dinaphtho[2,1-d:1′,2′-f][1,3,2]dithiazepine 3,3,5,5-tetraoxide
95%
- Product Code: 36162
CAS:
1242421-77-7
| Molecular Weight: | 819.64 g./mol | Molecular Formula: | C₃₆H₁₇F₁₂NO₄S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28009151 | |
| Melting Point: | 325-330°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in advanced organic synthesis and materials science due to its unique structural and electronic properties. Its application is prominent in the development of high-performance organic semiconductors, where its electron-deficient trifluoromethyl groups and rigid dinaphtho-dithiazepine framework contribute to enhanced charge transport properties. This makes it suitable for use in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs), where stability and efficiency are critical.
Additionally, its robust structure and electron-withdrawing characteristics make it a valuable ligand or building block in coordination chemistry, particularly for creating catalysts used in asymmetric synthesis. The compound's ability to stabilize metal centers and influence reaction pathways is leveraged in pharmaceutical and fine chemical manufacturing.
In supramolecular chemistry, it is employed to design functional materials with specific optical or electronic behaviors, such as sensors or molecular switches, due to its ability to form well-defined architectures and respond to external stimuli. Its fluorinated aromatic groups also make it a candidate for applications in hydrophobic coatings or membranes, where resistance to harsh chemical environments is required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿40,500.00 |
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(11bS)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]dinaphtho[2,1-d:1′,2′-f][1,3,2]dithiazepine 3,3,5,5-tetraoxide
This chemical is primarily utilized in advanced organic synthesis and materials science due to its unique structural and electronic properties. Its application is prominent in the development of high-performance organic semiconductors, where its electron-deficient trifluoromethyl groups and rigid dinaphtho-dithiazepine framework contribute to enhanced charge transport properties. This makes it suitable for use in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs), where stability and efficiency are critical.
Additionally, its robust structure and electron-withdrawing characteristics make it a valuable ligand or building block in coordination chemistry, particularly for creating catalysts used in asymmetric synthesis. The compound's ability to stabilize metal centers and influence reaction pathways is leveraged in pharmaceutical and fine chemical manufacturing.
In supramolecular chemistry, it is employed to design functional materials with specific optical or electronic behaviors, such as sensors or molecular switches, due to its ability to form well-defined architectures and respond to external stimuli. Its fluorinated aromatic groups also make it a candidate for applications in hydrophobic coatings or membranes, where resistance to harsh chemical environments is required.
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