261-92-7 Usage
Chemical class
Belongs to the class of benzothiazines.
Structure
Features a fused tricyclic ring system consisting of a pyridine ring fused to a benzothiazine ring.
Potential pharmaceutical applications
Known for its use as a pharmacological agent in the treatment of various diseases and disorders.
Biological activities
Exhibits diverse biological activities such as antiviral, anti-inflammatory, and anticancer properties.
Research focus
Studied for its potential use in the development of new drugs for the treatment of neurological and psychiatric disorders.
Unique structure
Its unique structure contributes to its diverse biological activities and makes it an interesting target for further research.
Drug development
10H-pyrido[4,3-b][1,4]benzothiazine is considered a promising candidate for the development of new drugs due to its potential pharmaceutical applications and diverse biological activities.
Further research
The compound's potential as a therapeutic agent warrants further investigation into its mechanisms of action, safety, and efficacy.
Molecular weight
The molecular weight of 10H-pyrido[4,3-b][1,4]benzothiazine is approximately 209.28 g/mol.
Check Digit Verification of cas no
The CAS Registry Mumber 261-92-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 261-92:
(5*2)+(4*6)+(3*1)+(2*9)+(1*2)=57
57 % 10 = 7
So 261-92-7 is a valid CAS Registry Number.
261-92-7Relevant academic research and scientific papers
Method for the production of azaphenothiazines
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, (2008/06/13)
6-aza-benzo[b]-phenothiazine derivatives having the formula, STR1 wherein X and Y can be any of hydrogen, lower alkyl, lower haloalkyl, carboxyl or carboxy alkyl are obtained through a reaction of 2-quinioline derivatives having the formula STR2 with a suitable 2-mercaptoaniline derivatives or dimers thereof under oxidative or free radical conditions. The 6-aza-benzo[b]-phenothiazine derivative are valuable precursors for pharmaceutically active substances such as pipacetate, isothioperdyl and prothiperdyl.
Process for the preparation of diaryl sulphides and diaryl selenides
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, (2008/06/13)
Diaryl sulphides and diaryl selenides of formula: where X=S or Se and Ar=aryl are made by the action of sulphur and sulphur dioxide or selenium and selenium dioxide on a compound of formula: The process is especially useful for the preparation of phenothiazines of formula STR1 in which X=S or Se and Z and Z1, which may be identical or different, are each hydrogen, halogen, alkyl or alkoxy.
