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Xanthen-9-yl hydroperoxide is a chemical compound with the molecular formula C13H9O3. It is a derivative of xanthene, a heterocyclic aromatic compound consisting of a benzene ring fused to a dihydrofuran ring. The hydroperoxide group (-OOH) is attached to the 9th carbon atom of the xanthene structure, making it a potentially reactive and unstable compound. Xanthen-9-yl hydroperoxide may be used in various chemical reactions and synthesis processes, particularly in the preparation of dyes and pigments. Due to its reactivity, it is essential to handle xanthen-9-yl hydroperoxide with caution and under appropriate safety measures.

18428-35-8

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18428-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18428-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,2 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18428-35:
(7*1)+(6*8)+(5*4)+(4*2)+(3*8)+(2*3)+(1*5)=118
118 % 10 = 8
So 18428-35-8 is a valid CAS Registry Number.

18428-35-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name xanthen-9-yl hydroperoxide

1.2 Other means of identification

Product number -
Other names xanthene hydroperoxide

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:18428-35-8 SDS

18428-35-8Relevant academic research and scientific papers

Synergistic effect of ketone and hydroperoxide in Bronsted acid catalyzed oxidative coupling reactions

Schweitzer-Chaput, Bertrand,Sud, Abhishek,Pinter, Aron,Dehn, Stefanie,Schulze, Philipp,Klussmann, Martin

supporting information, p. 13228 - 13232 (2014/01/06)

Waste not wasted: A mechanistic study of the autoxidative coupling of xanthene with cyclopentanone uncovered an autoinductive effect of the waste product hydrogen peroxide. It generates radicals in the presence of acid and ketones, which accelerate the reaction by providing an additional pathway to the reactive hydroperoxide intermediate. This discovery could be applied to achieve other Bronsted acid catalyzed oxidative coupling reactions.

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