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2-Phenoxymethyl-1,4-benzoquinone is a chemical compound with the molecular formula C14H10O3. It is a derivative of 1,4-benzoquinone, featuring a phenoxymethyl group attached to the 2-position of the benzoquinone ring. 2-Phenoxymethyl-1,4-benzoquinone is known for its potential applications in the synthesis of various organic compounds and pharmaceuticals, particularly as an intermediate in the production of certain drugs and dyes. Its structure provides a bridge between the quinone moiety, which is often involved in redox reactions, and the phenyl group, which can participate in a range of chemical transformations. The compound's properties, such as its reactivity and stability, make it a valuable building block in organic synthesis.

7714-50-3

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7714-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7714-50-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7714-50:
(6*7)+(5*7)+(4*1)+(3*4)+(2*5)+(1*0)=103
103 % 10 = 3
So 7714-50-3 is a valid CAS Registry Number.

7714-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(phenoxymethyl)cyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-Phenoxymethyl-1,4-benzochinon

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:7714-50-3 SDS

7714-50-3Relevant academic research and scientific papers

Palladium(II)-catalyzed synthesis of 2 H,3′ H -Spiro[benzofuran-3, 2′-naphthoquinones]

Claes, Pieter,Jacobs, Jan,Kesteleyn, Bart,Nguyen Van, Tuyen,De Kimpe, Norbert

, p. 8330 - 8339 (2013/09/24)

2H,3′H-Spiro[benzofuran-3,2′-naphthoquinones], constituting a new spiroheterocyclic skeleton, were synthesized starting from 2-aryloxymethyl-1,4-naphthoquinones by means of a palladium(II)-catalyzed reaction, which is a new spirocyclic transformation. Und

Pulse radiolytic kinetic study of the decay of α-methyl-substituted benzoquinone radical anions: A possible mechanistic model for bioreductive alkylation

O'Shea, Kevin E.,Fox, Marye Anne

, p. 611 - 615 (2007/10/02)

Pulse radiolysis and transient absorption spectroscopy were used to kinetically characterize the decay of several α-methyl-substituted 1,4-benzoquinone radical anions. Electron attachment rates, absorption spectra, extinction coefficients, and pKa/s

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