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Bis(4-methyl-3-pentenyl) ketone, also known as 1,6-hexanedione or methyl ethyl ketone peroxide, is an organic compound with the chemical formula C10H18O. It is a colorless liquid with a strong, pungent odor and is derived from the reaction of acetone with an alkyl peroxide. This ketone is widely used in the synthesis of various chemicals, such as fragrances, pharmaceuticals, and polymers. It is also employed as a crosslinking agent in the production of polyurethane foams and as a curing agent for unsaturated polyester resins. Due to its reactive nature, it is essential to handle bis(4-methyl-3-pentenyl) ketone with caution, as it can be hazardous and may cause irritation to the skin, eyes, and respiratory system.

2520-57-2

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2520-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2520-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2520-57:
(6*2)+(5*5)+(4*2)+(3*0)+(2*5)+(1*7)=62
62 % 10 = 2
So 2520-57-2 is a valid CAS Registry Number.

2520-57-2Downstream Products

2520-57-2Relevant academic research and scientific papers

Preparation of the Hexanolide Isolated from Conyza hypoleuca

Simonot, Bruno,Rousseau, Gerard

, p. 5723 - 5724 (1993)

A synthesis of racemic 13-hydroxy-10-sesquigeranic-1,12-olide is reported using bis(sym-collidine)iodine(I) hexafluorophosphate in the lactonisation key step.

AMORFRUTIN ANALOGS AS PPARGAMMA-MODULATORS

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Page/Page column 49; 50, (2014/11/13)

The present invention relates to Amorfrutin analogues and stereoisomeric forms, solvates, hydrates, conjugates and/or pharmaceutically acceptable salts of these compounds as well as pharmaceutical compositions containing at least one of these Amorfrutin analogues together with pharmaceutically acceptable carrier, excipient and/or diluents. Said Amorfrutin analogues have been identified as modulators of the peroxisome proliferator-activated receptors (PPARs), especially PPAR? and are useful for the prevention and treatment of metabolic diseases, inflammatory diseases, cancer and preparation of phytomedicals and/or functional food products for prevention of metabolic diseases.

Allylic alcohols as radical allylating agents. An overall olefination of aldehydes and ketones

Charrier, Nicolas,Quiclet-Sire, Beatrice,Zard, Samir Z.

scheme or table, p. 8898 - 8899 (2009/02/03)

2-Fluoropyridyl derivatives of allylic alcohols react with xanthates in the presence of lauroyl peroxide to give alkenes, often with high stereoselectivity. If the allylic alcohols are themselves derived from aldehydes or ketones, the overall process becomes a synthetic equivalent of the classical Wittig and related olefination reactions. Copyright

Stereo- and regioselectivity of intramolecular 1,2-arene-alkene photocycloaddition in 2-alkenyl-4-chromanones

Kalena, Govind P.,Pradhan, Padmanava,Banerji, Asoke

, p. 3209 - 3218 (2007/10/03)

Intramolecular 1,2-arene-alkene photocycloaddition of 2-alkenyl-4- chromanones gave complex multicyclic oxatetracyclotetradecanediones which on internal photo- and microwave induced thermal rearrangements provided a diverse array of compounds with [3.3.0]bicyclooctane carbon frame work. The stereo-and regiochemical aspects as well as desymmetrization of alkenyl chromanones due to intramolecular 1,2-arene-alkene photocycloaddition have also been discussed.

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