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7-Nitro-2-(trifluoromethyl)-10H-phenothiazine is a chemical compound belonging to the phenothiazine class, characterized by a tricyclic structure with a sulfur atom in the center. It features a nitro group at the 7-position and a trifluoromethyl group at the 2-position. 7-nitro-2-(trifluoromethyl)-10H-phenothiazine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in materials science. Due to its unique structure, it exhibits specific chemical and physical properties, making it a subject of interest for researchers in the field of organic chemistry.

2069-32-1

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2069-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2069-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2069-32:
(6*2)+(5*0)+(4*6)+(3*9)+(2*3)+(1*2)=71
71 % 10 = 1
So 2069-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H7F3N2O2S/c14-13(15,16)7-1-4-11-10(5-7)17-9-3-2-8(18(19)20)6-12(9)21-11/h1-6,17H

2069-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-nitro-2-(trifluoromethyl)-10H-phenothiazine

1.2 Other means of identification

Product number -
Other names EINECS 218-192-1

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 -
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More Details:2069-32-1 SDS

2069-32-1Downstream Products

2069-32-1Relevant academic research and scientific papers

SYNTHESIS OF SOME SUBSTITUTED 8-TRIFLUOROMETHYLNITROPHENOTHIAZINES

Malik, Seema,Anand, Madhu,Verma, S. S.,Prakash, L.,Mital, R. L.

, p. 201 - 214 (2007/10/02)

The synthesis of variedly ring substituted phenothiazines with two strong electron-withdrawing groups (trifluoromethyl and nitro) have been accomplished by the reactions of some reactive halonitrobenzenes with the zinc mercaptide of 2-amino-4-trifluoromethylbenzenethiol.The products have been characterised by elemental analysis, IR, 1H, 19F NMR and mass spectral studies.

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