Introduction of CAS:1003863-36-2 | Thieno[3,4-b]-1,4-dioxin-2-methanamine, 2,3-dihydro-
"1-{2H,3H-thieno[3,4-b][1,4]dioxin-2-yl}methanamine" is a chemical compound. It is related to other compounds such as "1-{2H,3H-thieno[3,4-b][1,4]dioxin-5-yl}ethan-1-one" and "Sodium 4-(2,3-dihydrothieno[3,4-b][1,4]dioxin-2-ylmethoxy)-1-butanesulfonate" .
Specification of CAS:1003863-36-2 | Thieno[3,4-b]-1,4-dioxin-2-methanamine, 2,3-dihydro-
|
ITEMS |
SPECIFICATION |
|
Density |
1.291±0.06 g/cm3(Predicted) |
|
Purity |
95% |
|
Boiling point |
276.6±28.0 °C(Predicted) |
|
Acidity coefficient (pKa) |
9.03±0.29(Predicted) |
Research Application of CAS:1003863-36-2 | Thieno[3,4-b]-1,4-dioxin-2-methanamine, 2,3-dihydro-
Scaffold for Drug Discovery
The compound hexahydro-2H-thieno[2,3-c]pyrrole, a related structure to 1-{2H,3H-thieno[3,4-b][1,4]dioxin-2-yl}methanamine, has been identified as a potential low molecular weight polar scaffold for the construction of compound libraries aimed at new drug discovery. Practical synthesis methods for derivatives of this scaffold have been developed, demonstrating its versatility in generating 3D-shaped molecule libraries for pharmaceutical research (Yarmolchuk et al., 2011).
Electrochromic Material Development
The synthesis and characterization of novel thiophene-based monomers, including derivatives of 2,5-di-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-ylthienyl, have been explored for their conducting and electrochromic properties. These compounds, functionalized with chromophore groups like azobenzene, coumarine, and fluorescein, exhibit significant changes in electronic and optoelectronic behaviors when polymerized, demonstrating their potential in developing electrochromic materials and devices (Yigit et al., 2014).
Photochromic and Electrochromic Polymers
Research into dithienylethene (DTE) and 3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine (didecyl-ProDOT) based materials has revealed their ability to switch between open and closed states upon light irradiation, with potential applications in photochromic and electrochromic devices. The emission properties of these compounds can be manipulated by light, offering new avenues for the development of responsive materials (Algi et al., 2015).



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