24133-88-8 Usage
General Description
2-Benzimidazolinone, 7-chloro-1-methyl- (8CI) is a chemical compound with the molecular formula C9H8ClN3O. It is a derivative of benzimidazole and is classified as an organic compound. This chemical is characterized by the presence of a benzimidazolinone core with a chlorine atom and a methyl group attached to it. It is used in various industrial and research applications as a building block for the synthesis of other organic compounds. Additionally, it has potential pharmaceutical properties and is being studied for its potential use in the development of new drugs. Due to its structural and functional properties, 2-Benzimidazolinone, 7-chloro-1-methyl- (8CI) has shown promise in various areas of chemical and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 24133-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,3 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24133-88:
(7*2)+(6*4)+(5*1)+(4*3)+(3*3)+(2*8)+(1*8)=88
88 % 10 = 8
So 24133-88-8 is a valid CAS Registry Number.
24133-88-8Relevant academic research and scientific papers
Spiroconjugated Tetraaminospirenes as Donors in Color-Tunable Charge-Transfer Emitters with Donor-Acceptor Structure
Grenz, David C.,Rose, Daniel,W?ssner, Jan S.,Wilbuer, Jennifer,Adler, Florin,Hermann, Mathias,Chan, Chin-Yiu,Adachi, Chihaya,Esser, Birgit
, (2021/12/22)
Charge-transfer emitters are attractive due to their color tunability and potentially high photoluminescence quantum yields (PLQYs). We herein present tetraaminospirenes as donor moieties, which, in combination with a variety of acceptors, furnished 12 charge-transfer emitters with a range of emission colors and PLQYs of up to 99 %. The spatial separation of their frontier molecular orbitals was obtained through careful structural design, and two DA structures were confirmed by X-ray crystallography. A range of photophysical measurements supported by DFT calculations shed light on the optoelectronic properties of this new family of spiro-NN-donor-acceptor dyes.