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2H-1,4-Benzothiazine, 2,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19195-32-5

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19195-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19195-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,9 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19195-32:
(7*1)+(6*9)+(5*1)+(4*9)+(3*5)+(2*3)+(1*2)=125
125 % 10 = 5
So 19195-32-5 is a valid CAS Registry Number.

19195-32-5SDS

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 2,3-diphenyl-4H-benzo[1,4]thiazine

1.2 Other means of identification

Product number -
Other names 2,3-Diphenyl-2H-1,4-benzothiazin

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:19195-32-5 SDS

19195-32-5Relevant academic research and scientific papers

From benzil arylimines to 2H-benzo-1,4-thiazines, benzothiazoles or indoles

Charrier, Jean-Damien,Landreau, Cyrille,Deniaud, David,Reliquet, Fran?oise,Reliquet, Alain,Meslin, Jean Claude

, p. 4195 - 4202 (2007/10/03)

A series of benzil monoarylimines (1) was treated with phosphorus pentasulfide in refluxing toluene or xylene. Thionation of 1 occurred readily to afford either 2H-benzo-1,4-thiazines (2) or indoles (4) via annulation reactions, depending strongly on the nature of the meta substituent of the arylamino group. Mechanisms for these rearrangements were proposed. Furthermore, subsequent oxidation of 2 provided benzothiazoles (3). All compounds were fully characterized by IR, MS, 13C and 1H NMR.

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