46815-10-5 Usage
Description
2-Ethylthiophenothiazine is a chemical compound that serves as a metabolite of thiethylperazine (T344495). It is characterized by the presence of a thiazole and a phenothiazine ring, which contribute to its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
2-Ethylthiophenothiazine is used as an active pharmaceutical ingredient for the development of anti-emetic drugs, specifically targeting pregnancy-related nausea and vomiting. Its efficacy in this application is attributed to its ability to alleviate symptoms without causing significant side effects.
Used in Antimicrobial Applications:
In the field of microbiology, 2-Ethylthiophenothiazine functions as a potent inhibitory agent against Enterococcus faecalis, a streptococcus Group D compound. Its antibacterial properties make it a valuable component in the development of new antibiotics to combat drug-resistant bacterial strains.
Overall, 2-Ethylthiophenothiazine is a versatile compound with applications in both the pharmaceutical and antimicrobial industries, offering potential benefits in the treatment of pregnancy-related nausea and the development of novel antibiotics.
Check Digit Verification of cas no
The CAS Registry Mumber 46815-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,8,1 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 46815-10:
(7*4)+(6*6)+(5*8)+(4*1)+(3*5)+(2*1)+(1*0)=125
125 % 10 = 5
So 46815-10-5 is a valid CAS Registry Number.
46815-10-5Relevant articles and documents
Combined KOH/BEt3Catalyst for Selective Deaminative Hydroboration of Aromatic Carboxamides for Construction of Luminophores
Li, Jinshan,Wang, Jiali,Yang, Jianguo,Yao, Wubing,Zhong, Aiguo
supporting information, p. 8086 - 8090 (2020/11/03)
The selective catalytic C-N bond cleavage of amides into value-added amine products is a desirable but challenging transformation. Molecules containing iminodibenzyl motifs are prevalent in pharmaceutical molecules and functional materials. Here we established a combined KOH/BEt3 catalyst for deaminative hydroboration of acyl-iminodibenzyl derivatives, including nonheterocyclic carboxamides, to the corresponding amines. This novel transition-metal-free methodology was also applied to the construction of Clomipramine and luminophores.
