21797-73-9 Usage
Structure
Phenothiazine ring with methyl groups at the 2 and 8 positions
A chemical structure featuring a phenothiazine ring (a tricyclic structure with two benzene rings and a sulfur atom) with two methyl groups attached, enhancing its properties.
3. Heterocyclic compound
A compound containing a ring of atoms with at least one heteroatom (an atom other than carbon) in the ring, contributing to its diverse chemical properties.
Pharmaceutical properties
Antipsychotic and antiemetic agent
2,8-dimethylphenoxathiine has been studied for its potential to treat mental disorders (antipsychotic) and prevent or alleviate nausea and vomiting (antiemetic).
5. Antioxidant properties
The compound has been investigated for its ability to neutralize free radicals, potentially protecting cells from oxidative damage.
6. Antibacterial properties
2,8-dimethylphenoxathiine has shown promise in fighting bacterial infections, making it a potential candidate for new antibacterial treatments.
7. Synthesis of organic compounds
The compound has been used as a building block in the creation of various organic molecules, demonstrating its versatility in chemical reactions.
8. Reagent in chemical reactions
2,8-dimethylphenoxathiine serves as a reagent, a substance that participates in a chemical reaction to facilitate the process or produce a desired product.
9. Applications in medicine and chemistry
The compound's diverse properties make it a promising candidate for various applications in both the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 21797-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,9 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21797-73:
(7*2)+(6*1)+(5*7)+(4*9)+(3*7)+(2*7)+(1*3)=129
129 % 10 = 9
So 21797-73-9 is a valid CAS Registry Number.
21797-73-9Relevant articles and documents
N-Benzyldithiocarbamate Salts as Sulfur Sources to Access Tricyclic Thioheterocycles Mediated by Copper Species
Luo, Bingling,Cui, Qingbin,Luo, Hongwen,Hu, Yumin,Huang, Peng,Wen, Shijun
supporting information, p. 2733 - 2738 (2016/09/13)
Using an easily prepared triethylammonium N-benzyldithiocarbamate salt as a sulfur source, a dual C?S functionalization of cyclic diaryliodoniums to form tricyclic thioheterocycles is realized. Our method uses the readily available copper sulfate to accelerate the chemical transformation under mild conditions. A broad range of cyclic diaryliodoniums with a ring size from 5- to 7-membered can be employed to gain a quick access to tricyclic thioheterocycles including dibenzothiophenes, thioxanthenes, and phenoxathiines. (Figure presented.).
Steps towards a practical synthesis of macrocyclic bisbenzylisoquinolines
Al-Hiari, Yusuf M.,Bennett, Stephen J.,Cox, Brian,Davies, Robert J.,Khalaf, Abedawn I.,Waigh, Roger D.,Worsley, Alan J.
, p. 647 - 659 (2007/10/03)
There are more than 400-reported bisbenzylisoquinoline alkaloids, many with interesting biological activity, but the reported syntheses are long and low yielding. As a result, there have been no systematic attempts at exploitation of the potential therapeutic applications. The concept of a sulfur 'stitch', restricting the conformational freedom of intermediates in the synthesis, will potentially allow analogues of the natural products to be prepared using relatively efficient routes. The synthesis of intermediate sulfur heterocycles is reported, based on 2,8-dimethylphenoxathiin, leading via 2,8-bis(bromomethyl) phenoxathiin-10,10-dioxide to a synthesis of 3,4,8,9-tetrahydro-13-oxa-6-thia-2, 10-diazapentacene, a key potential intermediate on the route to a variety of macrocyclic bisbenzylisoquinolines.
