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2-Hydroxyisophenoxazin-3-one is a chemical compound with the molecular formula C8H5NO3. It is a derivative of isophenoxazin-3-one, which is a heterocyclic compound containing oxygen and nitrogen atoms. 2-hydroxyisophenoxazin-3-one is characterized by the presence of a hydroxyl group (-OH) at the 2-position and a carbonyl group (C=O) at the 3-position. 2-Hydroxyisophenoxazin-3-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity. It can be used as an intermediate in the preparation of complex molecules, and its properties can be further explored for the development of new compounds with specific biological activities.

1915-49-7

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1915-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1915-49-7 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 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1915-49:
(6*1)+(5*9)+(4*1)+(3*5)+(2*4)+(1*9)=87
87 % 10 = 7
So 1915-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H7NO3/c14-9-5-8-12(6-10(9)15)16-11-4-2-1-3-7(11)13-8/h1-6,13H

1915-49-7SDS

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 2-Hydroxyisophenoxazin-3-one

1.2 Other means of identification

Product number -
Other names -

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:1915-49-7 SDS

1915-49-7Relevant academic research and scientific papers

Simple and efficient syntheses of 2-hydroxy-3H-phenoxazin-3-ones by aerobic oxidative cross-cyclocondensation in water

Li, Wenhao,Duan, Wenxue,Tang, Qingxuan,Li, Zhan-Ting,Yang, Guanyu

, p. 1136 - 1139 (2021)

A novel, simple and versatile synthetic approach that utilized natural renewable low-toxic gallic acid as an organocatalyst was developed for efficient aerobic oxidative cross-cyclocondensations of equimolar 2-aminophenols and 2-hydroxylphenols to afford various 2-hydroxy-phenoxazin-3-ones with moderate to high isolated yields at room temperature in water.

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.

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