1082549-89-0 Usage
Description
(9,9’-(5-(4,4,5,5-tetramethyl-1,2,3-dioxaborolan-2-yl)-1,3-phenylene)bis(9H-carbazole)) is a complex organic compound featuring two carbazole units connected by a 1,3-phenylene bridge, which includes a boron heteroatom. The molecule also incorporates a dioxaborolane group, a boron-containing heterocyclic compound. This chemical is notable for its potential applications in the field of materials science, particularly in the realm of organic electronic devices.
Uses
Used in Organic Electronic Devices:
(9,9’-(5-(4,4,5,5-tetramethyl-1,2,3-dioxaborolan-2-yl)-1,3-phenylene)bis(9H-carbazole)) is used as a component in the development of organic electronic devices due to its intriguing photophysical and electronic properties. Its unique structure contributes to the performance and efficiency of devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics.
Used in Organic Synthesis and Materials Chemistry:
In the field of Organic Synthesis and Materials Chemistry, (9,9’-(5-(4,4,5,5-tetramethyl-1,2,3-dioxaborolan-2-yl)-1,3-phenylene)bis(9H-carbazole)) serves as a valuable intermediate or building block for the synthesis of more complex molecules. The presence of the boron and dioxaborolane functionalities makes this compound particularly useful for various synthetic applications, where it can be further modified or used to create novel materials with tailored properties.
Used in the Pharmaceutical Industry:
While not explicitly mentioned in the provided materials, due to the structural complexity and the presence of a boron-containing group, (9,9’-(5-(4,4,5,5-tetramethyl-1,2,3-dioxaborolan-2-yl)-1,3-phenylene)bis(9H-carbazole)) could potentially be used in the pharmaceutical industry as a starting material for the development of new drugs, especially those that require boron-containing moieties for their biological activity.
Used in Research and Development:
In the Research and Development sector, (9,9’-(5-(4,4,5,5-tetramethyl-1,2,3-dioxaborolan-2-yl)-1,3-phenylene)bis(9H-carbazole)) is likely to be utilized for studying its fundamental properties, such as its reactivity, stability, and interactions with other molecules. This research could lead to a better understanding of how to harness its properties for various applications, including those not yet envisioned.
Check Digit Verification of cas no
The CAS Registry Mumber 1082549-89-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,2,5,4 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1082549-89:
(9*1)+(8*0)+(7*8)+(6*2)+(5*5)+(4*4)+(3*9)+(2*8)+(1*9)=170
170 % 10 = 0
So 1082549-89-0 is a valid CAS Registry Number.