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2,5-Difluoro-1,4-benzoquinone is a chemical compound characterized by the presence of two fluorine atoms at the 2nd and 5th positions of the 1,4-benzoquinone molecule. This organic compound belongs to the class of quinones, which are known for their ability to accept electrons and act as electron transporters in biological systems. The fluorine atoms in 2,5-difluoro-1,4-benzoquinone contribute to its unique electronic properties, potentially affecting its reactivity and stability compared to other benzoquinones. 2,5-Difluoro-1,4-benzoquinone may be of interest in various chemical and pharmaceutical applications due to its specific structural features and the influence of fluorine on its chemical behavior.

327-55-9

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327-55-9 Usage

Properties

yellow crystalline solid, sparingly soluble in water

Use

reagent in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals
Versatile building block for synthesis of various organic compounds
Potential applications in materials science and as a precursor for biologically active compounds

Check Digit Verification of cas no

The CAS Registry Mumber 327-55-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 327-55:
(5*3)+(4*2)+(3*7)+(2*5)+(1*5)=59
59 % 10 = 9
So 327-55-9 is a valid CAS Registry Number.

327-55-9SDS

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 2,5-Difluoro-1,4-benzoquinone

1.2 Other means of identification

Product number -
Other names 2,5-Difluor-p-benzoquinon

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:327-55-9 SDS

327-55-9Downstream Products

327-55-9Relevant academic research and scientific papers

Sulfogriseofulvin derivatives. Synthesis by [4+2]cycloaddition, structure, properties, crystal structure analysis, and antifungal activity of spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxides

Friedrich, Michael,Meichle, Wilhelm,Bernhard, Harald,Rihs, Grety,Otto, Hans-Hartwig

, p. 361 - 370 (2007/10/03)

Syntheses of substituted, especially of fluoro substituted benzoxathiole 1,1-dioxides, are described. These derivatives were transformed via the Peterson olefination into substituted 2-alkylidene derivatives 27. Diels-Alder reactions of 27 with 1,1-dimeth

Nitration of Strongly Deactivated Aromatics with Superacidic Mixed Nitric-Triflatoboric Acid (HNO3/2CF3SO3H-B(O3SCF3)3)

Olah, George A.,Orlinkov, Alexander,Oxyzoglou, Alexandros B.,Prakash, G. k. Surya

, p. 7348 - 7350 (2007/10/03)

The nitration of various deactivated arenes (including methanesulfonyl-, nitro-, and polyhalobenzenes) was carried out in good yield with mixed nitric-triflatoboric superacid.For example pentafluorobenzene gave pentafluoronitrobenzene in 99percent yield, nitrobenzene to m-dinitrobenzene in 92percent selectivity with 85percent overall yield, and methyl phenyl sulfone gave only the m-nitro isomer in 78percent isolated yield.Thus the new nitrating system gives high regioselectivity and yields under generally mild reaction conditions.The reagent system is compatible with many functional groups of arenes.

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