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6-HYDROXYBENZO(A)PHENOTHIAZIN-5-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25947-06-2

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25947-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25947-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,4 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25947-06:
(7*2)+(6*5)+(5*9)+(4*4)+(3*7)+(2*0)+(1*6)=132
132 % 10 = 2
So 25947-06-2 is a valid CAS Registry Number.

25947-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 12H-benzo[a]phenothiazine-5,6-dione

1.2 Other means of identification

Product number -
Other names 5H-Benzo[a]phenothiazin-5-one,6-hydroxy

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:25947-06-2 SDS

25947-06-2Relevant academic research and scientific papers

Synthesis and reactions of some new benzo[a]phenothiazine-3,4-dione derivatives

Abdel-Rahman,Kandeel,Berghot,Abdel-Motaal, Marwa

, p. 298 - 303 (2013/06/04)

The reaction of 2,3-dihydro-2,3-epoxy-1,4-naphthoquinone () with substituted anilines furnished the corresponding benzo[fused]heterocyclic derivatives. Furthermore, treatment of benzo[a]phenothiazine derivative with halo compounds, namely, ethyl bromoacetate, phenacyl bromide, dibromoethane, or chloroacetone afforded ether derivatives, respectively. Moreover, the reaction of with o-substituted aniline gave the corresponding benzo[a]phenothiazin-5-one derivatives and benzo[d][1,3]oxazin-4-one, respectively. Finally, the chromenone derivative was synthesized via the reaction of ester derivative with salicyaldhyde in refluxing pyridine. The newly synthesized compounds were characterized by spectroscopic measurements (IR, 1H NMR, 13C NMR, and mass spectra).

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