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1-Decanone, 2-hydroxy-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92989-69-0

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92989-69-0 Usage

Classification

Aromatic ketone This refers to the compound's classification as an aromatic ketone, which is a type of organic compound containing a ketone functional group and an aromatic ring.

Usage as flavoring agent

Food and cosmetic industries 1-Decanone, 2-hydroxy-1-phenylis commonly used as a flavoring agent in the food and cosmetic industries due to its pleasant aroma.

Usage as fragrance

Perfumes, soaps, and lotions The compound is also used as a fragrance in various personal care products, such as perfumes, soaps, and lotions, because of its sweet, floral, and slightly fruity scent.

Application in pharmaceuticals

Production of pharmaceuticals 1-Decanone, 2-hydroxy-1-phenylis used in the production of pharmaceuticals, indicating its importance in the development of medications.

Chemical intermediate

Organic synthesis processes The compound serves as a chemical intermediate in various organic synthesis processes, highlighting its versatility in chemical reactions and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 92989-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,8 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92989-69:
(7*9)+(6*2)+(5*9)+(4*8)+(3*9)+(2*6)+(1*9)=200
200 % 10 = 0
So 92989-69-0 is a valid CAS Registry Number.

92989-69-0Relevant academic research and scientific papers

Α - hydroxy ketone compound low priced high-efficient synthetic method

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Paragraph 0128-0131, (2017/08/25)

The invention discloses a cheap and efficient synthesis method of an alpha-hydroxyketone compound. The synthesis method is characterized in that a carbonyl compound undergoes an oxidation hydroxylation reaction at 10-120DEG C under normal pressure with iodine simple substance, N-bromosuccimide, copper bromide, bromine simple substance, hydrogen bromide, N-iodosuccimide or hydrogen iodide as a catalyst, sulfoxide as an oxidant, water or sulfoxide as a hydroxy source and sulfoxide, ethyl acetate, N,N-dimethyl formamide, acetonitrile, toluene, 1,4-dioxane, 1,2-dichloroethane, tetrahydrofuran or H2O as a solvent, and converts into the alpha-hydroxyketone compound in a high selectivity manner. Compared with traditional synthesis methods, the method disclosed in the invention has the advantages of simple operation, high yield, simple conditions, easy purification, small waste discharge amount, simple reaction apparatus, and easy industrial production. The method has wide applicability and can be used for synthesizing various alpha-hydroxyketone compounds.

Iodine promoted α-hydroxylation of ketones

Siddaraju, Yogesh,Prabhu, Kandikere Ramaiah

supporting information, p. 6749 - 6753 (2015/06/25)

A novel method for α-hydroxylation of ketones using substoichiometric amount of iodine under metal-free conditions is described. This method has been successfully employed in synthesizing a variety of heterocyclic compounds, which are useful precursors. α-Hydroxylation of diketones and triketones are illustrated. This strategy provides a novel, efficient, mild and inexpensive method for α-hydroxylation of aryl ketones using a sub-stoichiometric amount of molecular iodine.

I2- or NBS-catalyzed highly efficient α-hydroxylation of ketones with dimethyl sulfoxide

Liang, Yu-Feng,Wu, Kai,Song, Song,Li, Xinyao,Huang, Xiaoqiang,Jiao, Ning

supporting information, p. 876 - 879 (2015/04/14)

An efficient method for the direct preparation of high synthetic valuable α-hydroxycarbonyls is described. The simple and readily available I2 or NBS was used as catalyst. DMSO acts as the oxidant, oxygen source, and solvent. A diverse range of tertiary Csp3-H bonds as well as more challenging secondary Csp3-H bonds could be hydroxylated in this transformation. The reaction is mild, less toxic and easy to perform.

Oxazoles for click chemistry II: Synthesis of extended heterocyclic scaffolds

Patil, Pravin C.,Luzzio, Frederick A.,Demuth, Donald R.

, p. 3039 - 3041 (2015/05/27)

Abstract New routes to 2,4,5-trisubstituted oxazoles were established whereby the substitution pattern was established by the structure of the starting nonsymmetrical acyloins. 2-Chloromethyl-4, 5-disubstituted oxazoles were prepared by refinements of an earlier described process whereby chloroacetyl esters of symmetrical and nonsymmetrical acyloins were cyclized using an ammonium acetate/acetic acid protocol. After substitution is effected, the azide moiety is then installed by substitution under mild conditions. While dibrominated and iodinated phenyloxazoles are required for further synthetic elaboration, the cyclization reaction was found to be very sensitive to the relative positions of the halogens in the starting materials.

REACTIONS OF ACYL ANIONS GENERATED FROM ACID CHLORIDES AND DIIODOSAMARIUM

Souppe, J.,Namy, J-L.,Kagan, H.B.

, p. 2869 - 2872 (2007/10/02)

Acid chlorides react with SmI2 to give α-diketones.Various experiments show that the initially formed acyl radical is rapidly transformed into an acyl anion which is thus generated by quite an unusual route.This species acylates acid chlorides, aldehydes and ketones in situ to give α-diketones and α-diketols.There are some limitations to this acyl anion chemistry but the reactions are realized with a good efficiency at room temperature in THF solution.

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