10133-50-3

Usage

Uses

Used in Food and Beverage Industry:
4-(prop-1-en-2-yl)benzaldehyde is used as a natural flavoring agent for its sweet, spicy, and warm odor, enhancing the taste and aroma of various food and beverage products.
Used in Cosmetic Industry:
4-(prop-1-en-2-yl)benzaldehyde is used as a fragrance in the cosmetic industry, providing a pleasant scent to various cosmetic products.
Used in Pharmaceutical Industry:
4-(prop-1-en-2-yl)benzaldehyde is used as an antimicrobial and antioxidant ingredient in pharmaceuticals, contributing to the prevention of infections and oxidative stress.
Used in Personal Care Products:
4-(prop-1-en-2-yl)benzaldehyde is used as an antimicrobial and antioxidant ingredient in personal care products, promoting skin health and preventing infections.
Used in Medicine:
4-(prop-1-en-2-yl)benzaldehyde is used as a potential therapeutic agent for its anti-inflammatory and anti-cancer properties, offering potential benefits in the treatment of various medical conditions.

Upstream product

• 14559-87-6 isopropenylboronic acid 
• 1122-91-4 4-bromo-benzaldehyde 
• 6336-44-3 (E)-propenylboronic acid 
• 3457-45-2 p-formylacetophenone 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 26581-23-7 4-(1-methylethenyl)benzoic acid methyl ester 
• 3609-53-8 methyl 4-acetylbenzoate 
• 2077-19-2 2-(4-bromophenyl)propan-2-ol 
• 106-37-6 1.4-dibromobenzene 

Downstream Products

• 16262-48-9 1-(prop-1-en-2-yl)-4-vinylbenzene 

Relevant academic research and scientific papers

Novel Ketones from Roman Camomile Oil

β-Damascenone (1) has been identified in the fraction of Roman camomile (Anthemis nobilis) oil that contains homologues of carvotanacetone. 5-(3-Furyl)-2-methyl-1-penten-3-one (2), (E)-1-(2,6-dimethylphenyl)-2-buten-1-one (8), 4-isopropenylbenzaldehyde (4

Visible light-promoted dihydroxylation of styrenes with water and dioxygen

An efficient visible light promoted metal-free dihydroxylation of styrenes with water and dioxygen has been developed for the construction of vicinal alcohols. The protocol was operationally simple with a broad substrate scope. The mechanistic studies demonstrated that one of the hydroxyl groups came from water and the other one came from molecular oxygen. Additionally, the β-alkyoxy alcohols could also be obtained using a similar strategy.

Control of transient aluminum-aminals for masking and unmasking reactive carbonyl groups

A new reagent, the dimethylaluminum N,O-dimethylhydroxylamine complex, is effective at masking reactive carbonyl groups in situ from nucleophilic addition. This reagent allows chemoselective addition of reducing reagents, Grignard reagents, organolithiums, Wittig reagents, and enolates into substrates with multiple carbonyl groups. Moreover, the trapped carbonyl group, a stable aminal, can be unmasked in situ for additional synthetic manipulations.

Nickel-catalyzed cross-coupling of organogold reagents

Organogold compounds undergo nickel-catalyzed cross-coupling reactions with aryl and vinyl bromides in high yield under mild conditions. The reaction tolerates both electron-rich and electron-poor organogold complexes, and olefinic bromides undergo cross-coupling with high stereoselectivity. This novel transformation links well-established nickel catalysis with more recent developments in organogold transformations.

Suzuki cross-coupling reactions between alkenylboronic acids and aryl bromides catalysed by a tetraphosphane-palladium catalyst

A range of alkenylboronic acids undergo Suzuki cross-coupling with aryl bromides in good yields in the presence of [PdCl(C3H 5)]2/cis,cis,cis-1,2,3,4-tetrakis[(diphenylphosphanyl) methyl]cyclopentane as a catalyst. A wide variety of 1-arylprop-1-enes, 2-arylprop-1-enes, 2-arylbut-1-enes and 1,1-diarylethylene or styrene derivatives have been prepared. Moreover, the reaction tolerates several functions, such as acetyl, formyl, nitrile or nitro. Furthermore, this catalyst can be used at low loading, even for reactions of sterically hindered substrates. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.