10133-50-3

Basic information

• Product Name: 4-(prop-1-en-2-yl)benzaldehyde
• Synonyms: 4-(prop-1-en-2-yl)benzaldehyde
• CAS NO: 10133-50-3
• Molecular Formula: C₁₀H₁₀O
• Molecular Weight: 146.1858
• EINECS: -0
• Mol File: 10133-50-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(prop-1-en-2-yl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(prop-1-en-2-yl)benzaldehyde(10133-50-3)
• EPA Substance Registry System: 4-(prop-1-en-2-yl)benzaldehyde(10133-50-3)

Safety Data

• Hazardous Substances Data: 10133-50-3(Hazardous Substances Data)

Usage

General Description

4-(prop-1-en-2-yl)benzaldehyde, also known as cinnamaldehyde, is an organic compound with a chemical formula C9H8O. It is a yellow liquid with a sweet, spicy, and warm odor that is commonly used as a flavoring agent and fragrance in the food and cosmetic industries. Cinnamaldehyde is naturally occurring in cinnamon and other plants, and it is widely used as a natural flavoring agent in various food and beverage products. It also has antimicrobial and antioxidant properties, making it a valuable ingredient in pharmaceuticals and personal care products. Additionally, cinnamaldehyde has potential therapeutic effects, such as anti-inflammatory and anti-cancer properties, which have sparked interest in its potential use in medicine.

Upstream product

• 14559-87-6 isopropenylboronic acid 
• 1122-91-4 4-bromo-benzaldehyde 
• 6336-44-3 (E)-propenylboronic acid 
• 106-37-6 1.4-dibromobenzene 
• 2077-19-2 2-(4-bromophenyl)propan-2-ol 
• 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 

Downstream Products

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

Relevant articles and documents

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

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.

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.