製品名:2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene

IUPAC Name:4,4,5,5-tetramethyl-2-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl]-1,3,2-dioxaborolane

CAS番号:175361-81-6
分子式:C16H26B2O4S
純度:97%
カタログ番号:CM110000
分子量:336.06

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製品詳細

CAS番号:175361-81-6
分子式:C16H26B2O4S
融点:-
SMILESコード:CC1(C)C(C)(C)OB(C2=CC=C(B3OC(C)(C)C(C)(C)O3)S2)O1
密度:
カタログ番号:CM110000
分子量:336.06
沸点:434.3°C at 760 mmHg
MDL番号:MFCD09800563
保管方法:

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Organic Photodiode (OPD)
The most common type of organic photodetector is the organic photodiode (OPD). The photodiode has a simple structure in which an active layer is sandwiched between a transparent electrode and a metal electrode. In contrast to OLEDs, organic photodiodes (OPDs) utilize the organic semiconductor to absorb incident light and convert it to electric current. The structure and working principle are more like organic solar cells. Among the various organic photodetectors, organic photodiodes (OPDs) have been the most widely studied due to their fast response, high sensitivity, and full use of the existing research base of organic photovoltaics (OPVs).

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