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Oxacycloundecan-2-one, also known as 1,4,7,10-tetraoxacyclododecan-2-one, is a cyclic ketone with the molecular formula C7H12O4. It is a colorless to pale yellow liquid with a molecular weight of 160.17 g/mol. This chemical is characterized by its unique cyclic structure, which consists of a 12-membered ring with four oxygen atoms and two carbonyl groups. Oxacycloundecan-2-one is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the synthesis of macrocyclic compounds and as a chelating agent in metal extraction processes. Due to its reactivity and versatility, oxacycloundecan-2-one is an important building block in organic chemistry.

5579-79-3

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5579-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5579-79-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5579-79:
(6*5)+(5*5)+(4*7)+(3*9)+(2*7)+(1*9)=133
133 % 10 = 3
So 5579-79-3 is a valid CAS Registry Number.

5579-79-3Relevant academic research and scientific papers

A New Synthetic Method of Macrocyclic Lactones from ω-Iodoalkylacrylates

Abe, Motoji,Hayashikoshi, Takaoki,Kurata, Takeo

, p. 1789 - 1792 (2007/10/02)

When the photostimulated cyclization reaction of ω-iodoalkylacrylates was performed in the presence of metal hydride complexes such as sodium cyanoborohydride (NaBH3CN), sodium borohydride (NaBH4) and potassium borohydride (KBH4), the corresponding macrocyclic lactones were produced.The use of NaBH3CN led to the highest yield of lactones.

BAEYER-VILLIGER OXIDATION WITH Me3SiOOSiMe3 UNDER ASSISTANCE OF SnCl4 OR BF3-OEt2.

Matsubara,Takai,Nozaki

, p. 2029 - 2032 (2007/10/02)

Treatment of ketones with bis(trimethylsilyl) peroxide and Lewis acid such as SnCl//4 or BF//3-OEt//2 in dichloromethane at room temperature affords esters in fair to excellent yields. Jasmine lactone is synthesized from 2- left bracket (Z)-pentenyl right bracket cyclopentanine by means of Me//3SiOOSiMe//3-BF//3-OEt//2 system without any protection of the carbon-carbon double bond. The oxidation of enol acetates of ketones to alpha -hydroxy (or alpha -acetoxy) ketones with Me//3SiOOSiMe//3-FeCl//3 system is also disclosed.

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