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  Suraj Sharma,Bipul Sarma,Gakul Baishya New J. Chem. 2021 45 15475
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  Elizabeth J. Diana,U. S. Kanchana,Thomas V. Mathew Org. Biomol. Chem. 2021 19 7995
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  Jie Sheng,Jidan Liu,Liuqing Chen,Lingling Zhang,Liyao Zheng,Xingchuan Wei Org. Chem. Front. 2019 6 1471
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Phenol ethers
• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers
• Solvents and Organic Chemicals Organic Compounds Aldehyde/Ketone

2-Allyloxybenzaldehyde: A Comprehensive Overview

2-Allyloxybenzaldehyde, also known by its CAS number 28752-82-1, is a versatile organic compound with significant applications in various industries. This compound is characterized by its unique structure, which combines an aldehyde group with an allyloxy substituent on a benzene ring. The combination of these functional groups imparts 2-Allyloxybenzaldehyde with distinctive chemical properties, making it a valuable intermediate in organic synthesis and a key component in the production of specialty chemicals.

The chemical structure of 2-Allyloxybenzaldehyde consists of a benzene ring substituted with an aldehyde group at the para position and an allyl ether group at the ortho position. This arrangement not only enhances the compound's reactivity but also contributes to its stability under certain conditions. Recent studies have highlighted the potential of 2-Allyloxybenzaldehyde as a precursor for the synthesis of biologically active molecules, particularly in the pharmaceutical and agrochemical sectors.

In terms of physical properties, 2-Allyloxybenzaldehyde is typically a pale yellow liquid with a characteristic aromatic odor. It has a melting point of approximately -30°C and a boiling point around 160°C under standard atmospheric pressure. These properties make it suitable for use in various industrial processes, including polymerization reactions and flavoring agents.

The synthesis of 2-Allyloxybenzaldehyde can be achieved through several methods, including the oxidation of 2-allyloxytoluene or the coupling reaction of appropriate aldehydes and allyl ethers. Recent advancements in catalytic systems have enabled more efficient and environmentally friendly production methods, reducing the overall cost and improving yield.

2-Allyloxybenzaldehyde finds extensive applications in the flavor and fragrance industry, where it is used as a precursor for creating complex aromatic compounds. Additionally, it serves as an intermediate in the synthesis of pharmaceuticals, such as certain antibiotics and anti-inflammatory agents. The compound's ability to undergo various types of condensation reactions further enhances its utility in organic synthesis.

Recent research has focused on leveraging the unique reactivity of 2-Allyloxybenzaldehyde to develop novel materials with advanced properties. For instance, studies have demonstrated its potential as a building block for constructing conjugated polymers with applications in optoelectronics and sensors. Furthermore, investigations into its biodegradation pathways have provided insights into its environmental impact, paving the way for more sustainable industrial practices.

In conclusion, 2-Allyloxybenzaldehyde, with its CAS number 28752-82-1, remains a crucial compound in modern chemistry due to its diverse applications and promising research prospects. As scientific understanding continues to evolve, this compound is expected to play an even more significant role in driving innovation across various industries.

• 103811-70-7(Benzaldehyde, 2,5-bis(2-propenyloxy)-)
• 40359-61-3( )
• 96601-10-4(2,4-Bis(allyloxy)benzaldehyde)
• 19530-43-9(2-(ALLYLOXY)-1-NAPHTHALDEHYDE)
• 71186-58-8(Benzaldehyde, 4-methoxy-2-(2-propenyloxy)-)
• 918655-71-7(Benzaldehyde, 2,2'-[(2E)-2-butene-1,4-diylbis(oxy)]bis-)
• 918655-69-3(Benzaldehyde, 2,2'-[(2Z)-2-butene-1,4-diylbis(oxy)]bis-)
• 23343-06-8(2-(Allyloxy)-3-methoxybenzenecarbaldehyde)
• 140875-60-1(Benzaldehyde, 3-(hydroxymethyl)-5-methyl-2-(2-propenyloxy)-)
• 38002-87-8(2-[(2-methylprop-2-en-1-yl)oxy]benzaldehyde)