925240-83-1

Basic information

• Product Name: 2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde
• Synonyms: 2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde;Benzaldehyde, 2-[(1-methyl-2-propen-1-yl)oxy]-
• CAS NO: 925240-83-1
• Molecular Formula: C₁₁H₁₂O₂
• Molecular Weight: 176.21
• Mol File: 925240-83-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 282℃
• Flash Point: 122℃
• Appearance: /
• Density: 1.035
• CAS DataBase Reference: 2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde(925240-83-1)
• EPA Substance Registry System: 2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde(925240-83-1)

Safety Data

• Hazardous Substances Data: 925240-83-1(Hazardous Substances Data)

Usage

General Description

2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde is a chemical compound with the molecular formula C10H10O2. It is an organic compound that contains a benzene ring with an aldehyde group and a propenyl ether functional group. 2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde is commonly used in the production of fragrances, flavors, and other fine chemicals. It has a sweet, floral, and slightly fruity odor, making it a popular ingredient in perfumes and cosmetics. Additionally, it is also used in the synthesis of pharmaceuticals and as a flavoring agent in the food industry. However, 2-[(1-Methyl-2-propen-1-yl)oxy]benzaldehyde should be handled with caution as it may cause skin and eye irritation and should be stored in a cool, dry place away from heat and direct sunlight.

Upstream product

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Relevant articles and documents

Cascade Claisen and Meinwald Rearrangement for One-Pot Divergent Synthesis of Benzofurans and 2 H-Chromenes

A new cascade approach has been developed for the one-pot four-step divergent synthesis of polysubstituted benzofurans and 2H-chromenes, featuring a novel cascade aromatic Claisen rearrangement/Meinwald rearrangement/dehydrative or oxidative cyclization. This new method was demonstrated with 39 examples tolerating different substitutions at an epoxide, allylic ether, and aromatic ring, and we showcased its utility with the first total synthesis of natural product liparacid A in seven steps.

A cascade Claisen rearrangement/o-quinone methide formation/electrocyclization approach to 2H-chromenes

A new approach has been developed for the synthesis of 8-substituted 2H-chromenes, featuring a novel cascade aromatic Claisen rearrangement/o-quinone methide formation/6π-electrocyclization. This new method was demonstrated with 28 examples tolerating different substitutions at alkenes, allylic and aromatic ring and with total syntheses of three 2H-chromene natural products.