51238-86-9

Usage

Ketone derivative

A type of organic compound with a carbonyl functional group (C=O) 1-Pentanone, 3-methoxy-1,5-diphenyl- has a carbonyl group in its structure, which is characteristic of ketones.

Five-carbon chain

A straight chain of five carbon atoms The carbon backbone of 1-Pentanone, 3-methoxy-1,5-diphenyl- consists of five carbon atoms in a linear arrangement.

Phenyl group on each end

A benzene ring attached to each end of the carbon chain The molecule has a phenyl (a six-membered carbon ring with alternating single and double bonds) group attached to the first and last carbon atoms of the chain.

Commonly used as a solvent

Utilized in industrial and laboratory applications 1-Pentanone, 3-methoxy-1,5-diphenylis often employed as a solvent due to its ability to dissolve a variety of substances.

Production of pharmaceuticals and fragrances

Used in the synthesis and formulation of drugs and scented products This chemical compound is used as an intermediate or reactant in the production of pharmaceuticals and fragrances.

Sweet, floral odor

Characteristic pleasant and aromatic smell The compound is known for its sweet and floral scent, which makes it a popular choice for adding fragrance to consumer products.

Used in consumer products

Incorporated in perfumes, air fresheners, and scented products Due to its pleasant aroma, 1-Pentanone, 3-methoxy-1,5-diphenylis often used in products like perfumes and air fresheners to provide a desirable scent.

Potential applications in organic synthesis and chemical research

Unique structure and reactivity make it valuable for further study and development The compound's structure and its chemical reactivity open up opportunities for its use in creating new organic compounds and furthering scientific research.

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 67-56-1 methanol 
• 98-86-2 acetophenone 
• 122-78-1 phenylacetaldehyde 
• 60669-64-9 3-hydroxy-1,5-diphenylpentan-1-one 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 30076-98-3 (3,3-dimethoxypropyl)benzene 

Relevant academic research and scientific papers

FeCl3·6H2O-catalyzed mukaiyama-aldol type reactions of enolizable aldehydes and acetals

Mukaiyama-aldol type reactions of acetals derived from enolizable aldehydes with FeCl3·6H2O, an eco-friendly, low-cost, and stable catalyst, lead to β-methoxycarbonyl compounds with nearly quantitative yields. The methodology is extended to the parent aldehydes as starting materials, leading to the corresponding aldols with lower yields, but efficiently. Different alkyl and aryl substituted acetals and aldehydes have been tested in the reaction with linear and cyclic silyl enol ethers. Reactions are carried out in an open air atmosphere, and additives are not required. Acetals can be considered activating groups of the carbonyl moiety rather than a protecting group in this type of FeCl3·6H2O-catalyzed condensation.

NOVEL BETA-HYDROXYKETONES AND BETA-ALKOXYKETONES WITH ESTROGENIC ACTIVITY

This invention relates to β-hydroxyketones and β-alkoxyketones of formula (I), to their use as estrogen receptor modulators, and to methods for their preparation.

Synthesis and evaluation of estrogen agonism of diaryl 4,5- dihydroisoxazoles, 3-hydroxyketones, 3-methoxyketones, and 1,3-diketones: A compound set forming a 4D molecular library

In this paper, the preparation and systematic evaluation of estrogen receptor α (ERα) and estrogen receptor β (ERβ) activities of some diaryl-1,3-diones and their synthetic intermediates, diaryl-4,5-dihydroisoxazoles, diaryl-3-hydroxyketones, diaryl-3-met

L-proline-catalyzed one-pot three-component reaction for the synthesis of β-alkoxy ketones

β-Alkoxy ketones were prepared by a one-pot three-component reaction of aliphatic aldehydes, ketones, and alcohols catalyzed by L-proline. Steric effects on the reaction were studied with substituted ketones, aldehydes, and alcohols, and the results indicate that reactions employing methyl ketones, α-unsubstituted aliphatic aldehydes and methanol produce the β-alkoxy ketones in the best yields when L-proline is used as the catalyst. The reaction mechanism is discussed. Georg Thieme Verlag Stuttgart.

Selective aldol reactions of acetals on mesoporous silica catalyst

Mukaiyama-aldol reactions of carbonyl compounds with silyl enol ethers were well catalyzed on siliceous mesoporous materials (MCM-41). The reactivity of acetals was much higher than that of aldehyde. The reactions proceeded selectively at 273-298 K on the

Chemoselective aldol reaction of silyl enolates catalyzed by Mgl2 etherate

(matrix presented) Mukaiyama-type aldol coupling of typical silyl enolates 2-4 with aryl or vinyl aldehydes and acetals was realized in the presence of 1-5 mol % of MgI2 etherate (1) in a mild, efficient, and highly chemoselective manner. Iodid

Reversal Phenomena of the Preferential Activation of Aldehydes to the Corresponding Acetals under Non-Basic Conditions. The Chemoselective Aldol Reaction of Aldehydes with t-Butyldimethylsilyl Enol Ethers Using TBSCl-InCl3 as a Catalyst

In the presence of a catalytic amount of t-butyldimethylsilyl chloride (TBSCl) and indium(III) chloride (InCl3), aldehydes smoothly react with t-butyldimethylsilyl enol ethers to afford the corresponding aldol adducts in good yields whereas acetals do not

Efficient Activation of Acetals, Aldehydes, and Imines toward Silylated Nucleophiles by the Combined Use of Catalytic Amounts of 2 and TMS-CN under Almost Neutral Conditions

In the presence of catalytic amount of a transition metal compound such as 2, Co(acac)2, or NiCl2, trimethylsilyl cyanide smoothly reacts with acetals to form α-methoxy carbonitriles in good yields.In the coexistence of catalytic amounts of Rh

Efficient Activation of Acetals toward Nucleophiles with 2 Catalyst. New Method for the Preparation of Aldols from Acetals and Silyl Enol Ethers by the Combined Use of Catalytic Amounts of 2 and Trimethylsilyl Cyanide

In the presence of a catalytic amount of 2, di-μ-chloro-bis(1,5-cyclooctadiene)dirhodium, trimethylsilyl cyanide smoothly reacts with acetals derived from aliphatic, unsaturated and aromatic aldehydes to form the corresponding α-cyano derivativ