29241-15-4 Usage
Family
Benzothiadiazole family of organic compounds
Structure
Presence of a benzene ring fused to a thiadiazole ring
Functional groups
Chlorine atom at the 5th position
Organic electronic materials
Used in the synthesis of organic semiconductors and conducting polymers
Dye-sensitized solar cells
Studied for potential applications due to favorable electronic and optical properties
Organic light-emitting diodes
Investigated for use in light-emitting devices
Anti-cancer agent
Shown promise in scientific research as a potential cancer-fighting compound
Electron-accepting properties
Contributes to its use in organic electronic materials
Electronic and optical properties
Favorable for applications in solar cells and light-emitting diodes
Check Digit Verification of cas no
The CAS Registry Mumber 29241-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29241-15:
(7*2)+(6*9)+(5*2)+(4*4)+(3*1)+(2*1)+(1*5)=104
104 % 10 = 4
So 29241-15-4 is a valid CAS Registry Number.
29241-15-4Relevant articles and documents
Method for continuously synthesizing benzothiadiazole compound
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Paragraph 0031-0034, (2020/06/02)
The invention discloses a method for continuously synthesizing a benzothiadiazole compound, comprising the following step: by using an o-mercaptoaniline compound, sodium nitrite and water as reactionsubstrates in a continuous flow reactor, a diazotization-coupling reaction is carried out at certain temperature under certain pressure to obtain the benzothiadiazole compound. By adopting the technology, no protonic acid participates, and water is used as a reactant and a solvent, so that the method is green and environment-friendly. The continuous flow reactor is used, online materials are small, the process is intrinsically safe, and the method is suitable for large-scale production.
