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79253-81-9

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79253-81-9 Usage

Molecular structure

12-phenyl-12H-indolo[1,2-b][1,2]benzothiazin-12-ol 5,5-dioxide consists of a benzothiazine ring system, an attached phenyl group, and a fused indole ring.

Functional group

The compound contains a 5,5-dioxide functional group, which may contribute to its potential pharmacological and biochemical properties.

Complexity

The compound has a complex and specific structure, which may be responsible for its unique biological activities.

Pharmacological applications

12-phenyl-12H-indolo[1,2-b][1,2]benzothiazin-12-ol 5,5-dioxide has potential pharmacological applications due to its unique structure and possible specific biological activities.

Biochemical applications

The compound may also have potential biochemical applications, as its structure could impart specific interactions with biological systems.

Research and studies

Further research and studies are needed to fully understand the properties and potential uses of 12-phenyl-12H-indolo[1,2-b][1,2]benzothiazin-12-ol 5,5-dioxide. This includes exploring its interactions with biological systems, potential therapeutic effects, and possible side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 79253-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,5 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79253-81:
(7*7)+(6*9)+(5*2)+(4*5)+(3*3)+(2*8)+(1*1)=159
159 % 10 = 9
So 79253-81-9 is a valid CAS Registry Number.

79253-81-9SDS

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 5,5-dioxo-12-phenylindolo[1,2-b][1,2]benzothiazin-12-ol

1.2 Other means of identification

Product number -
Other names 12-Phenyl-12H-indolo[1,2-b][1,2]benzothiazin-12-ol 5,5-dioxide

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:79253-81-9 SDS

79253-81-9Downstream Products

79253-81-9Relevant articles and documents

Dilithiation of 1-Benzenesulfonylindoles

Sundberg, Richard J.,Broome, Rita,Walters, Claudia Powers,Schnur, Dora

, p. 807 - 809 (2007/10/02)

Benzenesulfonylindole is converted to a dilithio derivative by 2.2 equivalents of lithiating reagent.The dilithio derivative gives rise to sultones on reaction with carbonyl compounds.This reaction proceeds by an intramolecular displacement of the indole group from the bis-adduct.Fair to poor yields of the 2-indolylcarbinols can also be isolated.Benzoyl chloride forms a thiazine dioxide ring by addition at both the 2-indolyl and 2'-phenylsulfonyl positions. 3-Methyl-1-benzenesulfonylindole is also easily dilithiated.

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