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Phenoxazinone, a member of the phenoxazines family, is a chemical compound characterized by its molecular formula C12H7NO. It is a yellow powder that is insoluble in water and is recognized for its potential applications in both industrial and medicinal fields.

1916-63-8

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1916-63-8 Usage

Uses

Used in Textile Industry:
Phenoxazinone is used as a dye or pigment for coloring textiles, due to the vibrant red and blue colors produced by its derivatives.
Used in Paper Industry:
Phenoxazinone is used as a dye or pigment for coloring paper, contributing to the production of visually appealing paper products.
Used in Cosmetics Industry:
Phenoxazinone is used as a dye or pigment for coloring cosmetics, enhancing the appearance of various cosmetic products.
Used in Pharmaceutical Research:
Phenoxazinone is studied for its potential antioxidant and anti-inflammatory properties, suggesting it may have therapeutic benefits in the treatment of various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1916-63-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1916-63:
(6*1)+(5*9)+(4*1)+(3*6)+(2*6)+(1*3)=88
88 % 10 = 8
So 1916-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H7NO2/c14-8-5-6-10-12(7-8)15-11-4-2-1-3-9(11)13-10/h1-7H

1916-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name phenoxazin-3-one

1.2 Other means of identification

Product number -
Other names phenoxazone

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:1916-63-8 SDS

1916-63-8Relevant academic research and scientific papers

Reaction of o-Aminophenol and p-Benzoquinone in Acetic Acid

Bolognese, Adele,Scherillo, Giulia,Schaefer, Wolfram

, p. 1003 - 1006 (2007/10/02)

The reaction of o-aminophenol and p-benzoquinone in acetic acid yields phenoxazinones 1, 5 and 6, phenoxazine 7, triphenodioxazine 2, ditriphenodioxazine 3 and the phenoxazinonyltriphenodioxazine 4.

A NEW SYNTHESIS OF 3H-PHENOXAZIN-3-ONES

Bird, C. W.,Latif, M.

, p. 529 - 534 (2007/10/02)

The reductive cyclisation of 3-hydroxy-2'-nitrodiphenyl ethers provides a new synthesis of 3H-phenoxazin-3-ones, which should be particularly suitable for the synthesis of actinomycins.

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