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2913-48-6

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2913-48-6 Usage

Derived from

cyclohexadiene

Contains

a hydroxyl group and a methyl group

Usage

in the synthesis of various organic compounds, intermediate in the production of pharmaceuticals and agrochemicals

Known for

antioxidant properties, potential applications in medicine and food preservation

Reactivity

can undergo various chemical reactions, versatile building block in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 2913-48-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2913-48:
(6*2)+(5*9)+(4*1)+(3*3)+(2*4)+(1*8)=86
86 % 10 = 6
So 2913-48-6 is a valid CAS Registry Number.

2913-48-6SDS

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-hydroxy-3-methylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-Me-3-OH-p-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:2913-48-6 SDS

2913-48-6Relevant articles and documents

Complex reaction dynamics in the cerium-bromate-2-methyl-1,4-hydroquinone photoreaction

Bell, Jeffrey G.,Green, James R.,Wang, Jichang

, p. 9795 - 9800 (2014)

Spontaneous oscillations with a long induction time were observed in the bromate-2-methyl-1,4-hydroquinone photoreaction in a batch reactor, where removal of illumination effectively quenched any reactivity. A substantial lengthening of the oscillatory window and a dramatic increase in the complexity of the reaction behavior arose upon the addition of cerium ions, in which separate bifurcation regions and mixed mode oscillations were present. The complexity has a strong dependence on the intensity of illumination supplied to the system and on the initial concentrations of the reactants. 1H NMR spectroscopy measurements show that the photoreduction of 2-methyl-1,4-benzoquinone leads to the formation of 2-methyl-1,4-hydroquinone and the compound 2-hydroxy-3-methyl-1,4-benzoquinone. Spectroscopic investigation also indicates that the presence of methyl group hinders the bromination of the studied organic substrate 2-methyl-1,4-hydroquinone, resulting in the formation of 2-methyl-1,4-benzoquinone.

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