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4-hydroxy-5-phenylcyclohexa-3,5-diene-1,2-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23305-16-0

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23305-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23305-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,0 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23305-16:
(7*2)+(6*3)+(5*3)+(4*0)+(3*5)+(2*1)+(1*6)=70
70 % 10 = 0
So 23305-16-0 is a valid CAS Registry Number.

23305-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-5-phenylcyclohexa-3,5-diene-1,2-dione

1.2 Other means of identification

Product number -
Other names 2-hydroxy-5-phenylcyclohexa-2,5-diene-1,4-dione

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:23305-16-0 SDS

23305-16-0Upstream product

23305-16-0Downstream Products

23305-16-0Relevant academic research and scientific papers

A divergent and selective synthesis of ortho- and para-quinones from phenols

Huang, Zheng,Kwon, Ohhyeon,Esguerra, Kenneth Virgel N.,Lumb, Jean-Philip

, p. 5871 - 5885 (2015/08/04)

Abstract We describe a divergent synthesis of substituted ortho- and para-quinones by catalytic aerobic oxygenation of phenols. Substituted quinones are omnipresent in chemistry and biology, but their synthesis frequently suffers from low efficiency and poor scope. Our methodology employs a catalytic aerobic di-functionalization of phenols to aryloxy-ortho-quinones. Regioselective substitution with an alcohol provides the alkoxy substituted ortho- or para-quinone, while hydrolysis affords the para-hydroxyquinone. These are mild and selective conditions for the synthesis of diversely substituted quinones from readily available phenol starting materials.

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