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1,3-dinitro-10H-phenoxazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26103-32-2

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26103-32-2 Usage

Derivative of

Phenoxazine

Functional groups

Contains two nitro functional groups

Application

Used as a fluorescent dye

Color

Intense red

Useful in

Biological and cellular imaging

Potential use

Studied for its potential as an electron transporting material in organic electronic devices

Chemical properties

Unique chemical properties

Value

Versatile and valuable compound in scientific research and industrial uses

Check Digit Verification of cas no

The CAS Registry Mumber 26103-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26103-32:
(7*2)+(6*6)+(5*1)+(4*0)+(3*3)+(2*3)+(1*2)=72
72 % 10 = 2
So 26103-32-2 is a valid CAS Registry Number.

26103-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dinitro-10H-phenoxazine

1.2 Other means of identification

Product number -
Other names 1,3-Dinitrophenoxazin

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:26103-32-2 SDS

26103-32-2Downstream Products

26103-32-2Relevant academic research and scientific papers

Reactions of ortho-aminophenols and ortho-aminothiophenols with 1,3,5-trinitrobenzene

Dutov, Mikhail D.,Vorob'ev, Sergei S.,Serushkina, Ol'ga V.,Shevelev, Svyatoslav A.,Ugrak, Bogdan I.,Kachala, Vadim V.

, p. 230 - 232 (2006)

1,3-Dinitrophenoxazine and 1,3-dinitrophenothiazine derivatives were prepared by the reactions of ortho-aminophenols and ortho-aminothiophenols with 1,3,5-trinitrobenzene.

SPIROCYCLIC MEISENHEIMER COMPLEXES. XIII. INTRAMOLECULAR NUCLEOPHILIC SUBSTITUTION OF THE NITRO GROUP DURING CYCLIZATION OF SOME o-HYDROXYPHENYLPICRAMIDES TO PHENOXAZINES

Knyazev, V. N.,Drozd, V. N.,Mozhaeva, T. Ya.

, p. 770 - 775 (2007/10/02)

The intramolecular nucleophilic cyclization of o-hydroxyphenylpicramides to the corresponding phenoxazines occurs without a previous Smiles rearrangement.If a methyl group is introduced into the picryl ring only the nitro group in the ortho (and not the p

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