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261-92-7

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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.

261-92-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 10H-pyrido[4,3-b][1,4]benzothiazine

1.2 Other means of identification

Product number -
Other names 10H-benzo[b]pyrido[3,4-e][1,4]thiazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:261-92-7 SDS

261-92-7Relevant articles and documents

Method for the production of azaphenothiazines

-

, (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.

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