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2,3-Dimethyl-5-acetoxymethyl-p-benzoquinone is a para-benzoquinone derivative, a yellow crystalline solid with significant applications in organic synthesis and potential medicinal uses.
Used in Organic Synthesis:
2,3-Dimethyl-5-acetoxymethyl-p-benzoquinone is used as a reagent for the selective oxidation of alcohols to carbonyl compounds, a critical step in the synthesis of various organic compounds.
Used in Material Preparation:
In the industry of material science, 2,3-Dimethyl-5-acetoxymethyl-p-benzoquinone is used as a co-catalyst in the preparation of organic materials such as resins, polymers, and adhesives, enhancing their properties and performance.
Used in Pharmaceutical Research:
2,3-Dimethyl-5-acetoxymethyl-p-benzoquinone is studied for its potential as an anti-tumor agent in the pharmaceutical industry, due to its ability to induce apoptosis in cancer cells, offering a new avenue for cancer treatment.
Safety Note:
Proper safety precautions should be observed when handling 2,3-Dimethyl-5-acetoxymethyl-p-benzoquinone, as it can pose hazards if not used responsibly, highlighting the importance of safety in research and industrial applications.

40870-69-7

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40870-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40870-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,7 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40870-69:
(7*4)+(6*0)+(5*8)+(4*7)+(3*0)+(2*6)+(1*9)=117
117 % 10 = 7
So 40870-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O4/c1-6-7(2)11(14)9(4-10(6)13)5-15-8(3)12/h4H,5H2,1-3H3

40870-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4,5-dimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)methyl acetate

1.2 Other means of identification

Product number -
Other names p-Benzoquinone,2,3-dimethyl-5-(hydroxymethyl)-,acetate (ester)

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:40870-69-7 SDS

40870-69-7Relevant academic research and scientific papers

Choice of Manganese(III) Complexes for the Synthesis of 4,4'-Biphenyldiols and 4,4'-Diphenoquinones

Nishino, Hiroshi,Nobuyuki, Itoh,Nagashima, Makiko,Kurosawa, Kazu

, p. 620 - 622 (2007/10/02)

2,6-Disubstituted phenols are oxidized with tris(2,4-pentanedionato)manganese(III), , in glacial acetic acid to give the corresponding 4,4'-biphenyldiols in high yields, whereas similar reactions using manganase(III) acetate, , instead of quantitatively yield the corresponding 4,4'-diphenoquinones.Cross-coupling reactions of 2,6-di-t-butylphenol and other substituted phenols afford the corresponding cross-coupled 4,4'-biphenyldiols and 4,4'-diphenoquinones together with oxidation products derived from them starting phenols themselves.The advantageous use of and Mn(OAc)3> in the ubiqitous phenol coupling reaction is discussed.

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