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30725-13-4

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30725-13-4 Usage

General Description

10H-Phenoxazin-3-amine, also known as 3-Amino-10H-phenoxazine, is a chemical compound with the molecular formula C12H9N3O. It is a heterocyclic aromatic amine with a phenoxazine core and an amino group at the 3-position. 10H-Phenoxazin-3-aMine has applications as a redox indicator, particularly in analytical chemistry, where it is used to detect the presence of hydrogen peroxide. It is also used in the synthesis of various organic compounds and as a fluorescent dye in biological and medical research. 10H-Phenoxazin-3-amine has been studied for its potential use in chemiluminescent assays and as a reactant in organic synthesis. Despite its potential utility, it is important to handle this compound with caution, as it may be harmful if ingested or inhaled and can cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 30725-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,2 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30725-13:
(7*3)+(6*0)+(5*7)+(4*2)+(3*5)+(2*1)+(1*3)=84
84 % 10 = 4
So 30725-13-4 is a valid CAS Registry Number.

30725-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 10H-Phenoxazin-3-amine

1.2 Other means of identification

Product number -
Other names 10H-phenoxazin-3-ylamine

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:30725-13-4 SDS

30725-13-4Downstream Products

30725-13-4Relevant articles and documents

Further studies on the cyclisation of 3-hydroxy-2'-nitrodiphenyl ethers and related compounds

Bird,Latif

, p. 1813 - 1816 (2007/10/02)

The reductive cyclisation of 4,6-dimethyl and 4,6-dichloro derivatives of 3-hydroxy-2'-nitrodiphenyl ethers has been examined as a potential route to 1H-phenoxazinones. Unexpectedly, cyclisation of the dichloro compound proceeded with loss of a Cl and yielded 2-chloro-3H-phenoxazin-3-one. The cyclisation of a range of analogous substrates has been investigated and shown to provide novel and convenient syntheses of 3-amino-phenoxazine, 3H-phenothiazin-3-one and 8-hydroxy-5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one.

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