107274-11-3

Usage

Class of compound

Ketones It belongs to the class of ketones, which are organic compounds with a carbonyl group (C=O) bonded to two carbon-containing groups.

Structure

Five-carbon chain with a ketone group and two phenyl groups The compound has a linear structure consisting of a five-carbon chain with a ketone group (C=O) at the first carbon and two phenyl groups (aromatic rings with a hydrogen atom attached to each carbon) attached to the first and fifth carbons.

Hydroxyl group

One of the phenyl groups has a hydroxyl (OH) group attached The phenyl group attached to the fifth carbon of the chain contains a hydroxyl group, which is a polar functional group that can form hydrogen bonds.

Precursor in synthesis

Commonly used as a precursor in the synthesis of other organic compounds Due to its unique structure, 1-Pentanone, 5-hydroxy-1,5-diphenylis often used as a starting material for the synthesis of more complex organic molecules.

Applications

Production of pharmaceuticals, fragrances, and dyes The compound is used in the production of various products, including pharmaceuticals, fragrances, and dyes, due to its ability to be converted into a wide range of organic compounds.

Industrial use

Solvent in various industrial processes 1-Pentanone, 5-hydroxy-1,5-diphenylis also used as a solvent in different industrial processes, taking advantage of its solubility and reactivity properties.

Building block for complex organic molecules

Unique structure and properties make it a valuable building block The compound's structure and properties make it an important intermediate for the synthesis of complex organic molecules, which can be further modified or functionalized to create a variety of products.

Upstream product

• 42512-76-5 5-hydroxy-1,5-diphenyl-pent-2-yn-1-one 
• 109395-25-7 5-bromo-1,5-diphenyl-pentan-1-one 
• 6263-83-8 1,5-diphenyl-1,5-pentanedione 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 38858-73-0 1-phenyl-1-trimethylsiloxycyclopropane 
• 98-86-2 acetophenone 
• 29526-96-3 1-phenylcyclopropan-1-ol 
• 100-42-5 styrene 
• 10413-00-0 5-oxo-5-phenylpentanenitrile 
• 10413-05-5 5-hydroxy-5-phenylpentanenitrile 
• 100-58-3 phenylmagnesium bromide 
• 622860-41-7 trans-1,5-diphenyl-4-penten-1-ol 
• 1130680-70-4 (Z)-1,5-diphenylpent-4-en-1-ol 
• 42512-63-0 1,5-diphenylpent-2-yne-1,5-diol 

Downstream Products

• 6263-83-8 1,5-diphenyl-1,5-pentanedione 
• 5449-44-5 1,5-diphenyl-pentane-1,5-diol 
• 55696-62-3 meso-1,5-diphenyl-pentane-1,5-diol 
• 195443-92-6 (-)-(S,S)-1,5-diphenylpentane-1,5-diol 

Relevant academic research and scientific papers

Iron-Catalyzed Ring-Opening Reactions of Cyclopropanols with Alkenes and TBHP: Synthesis of 5-Oxo Peroxides

The ring opening of cyclopropanols is rarely used in multicomponent reactions. Herein we report the three-component reaction of cyclopropanols with alkenes and tert-butyl hydroperoxide (TBHP) catalyzed by an iron catalyst. This protocol enables the incorporation of both the β-carbonyl fragment and a peroxy unit across the C=C double bond regioselectively, thus allowing an efficient, facile access to 5-oxo peroxides. Modification of the biologically active molecules and various downstream derivatizations of the peroxides are also demonstrated.

Method for synthesizing alkyne through catalytic asymmetric cross coupling (by machine translation)

The invention belongs to the field of, asymmetric synthesis, and discloses a method for catalyzing asymmetric cross- coupling to synthesize: an alkyne, and the L method comprises, the following steps, of A: preparing B a cuprous, salt and C a: ligand; preparing a catalyst; adding a base; reacting the compound with the compound with the compound; and reacting the compound with the compound. Of these, one of them, X is selected from the group consisting of, R halogens. 1 Optionally substituted heteroarylsulfonylcyanamide groups selected from the, group consisting, of optionally substituted, phenyl groups In-flight vehicle, R6 Trialkyl silyl groups or alkyl radicals, R2 Cycloalkyl radicals optionally substituted with an, optionally substituted alkyl, (CH radical2 )n R4 Multi,layer chain, n＝0-10,R saw blade4 A group selected, from, the group consisting of phenyl, alkenyl, aralkynyls, noonyloxy,and, noonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylphenyl disiloxy-radicals. R3 A ligand, selected from hydrogen or any of the functional groups, is selected from the group consisting of, hydrogen and any L other functional group. The method, R disclosed by the, A invention has the, advantages of good catalytic, R ’ effect, wide application range. and high catalytic efficiency, and the, method disclosed by the, invention has the. advantages of good catalytic effect, wide application range and high catalytic efficiency. (by machine translation)

Cobalt-catalyzed aerobic oxidation of (E)- and (Z)-bishomoallylic alcohols

Stereoselectivity for (5-phenyltetrahydrofur-2-yl)alkan-1-ol formation (cis:trans 1:99) from 5-methyl- and 5-phenyl-substituted 1-phenylpent-4-en-1-ols via cobalt-catalyzed aerobic oxidation was independent of the olefinic π-bond configuration of the su

Is it possible to estimate the enantioselectivity of a chiral catalyst from its racemic mixture?

The evaluation of a racemic catalyst was investigated in the case of oxazaborolidine (OAB)-catalyzed borane reduction of 1,5-diphenyl-1,5-pentanedione, giving the corresponding diol. On the basis of the diastereoselectivity of the diols, it is possible to estimate the enantioselectivity (ee) of the first step, which correlates well with the ee in the reaction of the structurally similar phenyl n-pentyl ketone with enantiopure OAB catalyst. The measure of diastereoselectivity could be a tool for screening racemic catalysts without the need for resolving the individual enantiomers, if in the second step of the process there is no substrate control and no catalyst scrambling. Copyright

Stereocontrol between remote atom centers in acyclic substrates. Anti addition of hydride to 1,5-, 1,6-, and 1,7-hydroxy ketones

For conformationally unconstrained, acyclic organic compounds, the control of stereogenic centers at remote positions of a chain, that is, at a distance of four or more atom centers, remains a challenging problem in asymmetric synthesis. We report on our