871878-99-8

Basic information

• Product Name: 1-(2,4-dimethoxyphenyl)-2-hydroxyethanone
• Synonyms: 1-(2,4-dimethoxyphenyl)-2-hydroxyethanone
• CAS NO: 871878-99-8
• Molecular Weight: 196.203
• Mol File: 871878-99-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(2,4-dimethoxyphenyl)-2-hydroxyethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-dimethoxyphenyl)-2-hydroxyethanone(871878-99-8)
• EPA Substance Registry System: 1-(2,4-dimethoxyphenyl)-2-hydroxyethanone(871878-99-8)

Safety Data

• Hazardous Substances Data: 871878-99-8(Hazardous Substances Data)

Usage

Description

1-(2,4-dimethoxyphenyl)-2-hydroxyethanone, also known as 2,4-dimethoxybenzaldehyde, is an organic compound characterized by its molecular formula C10H12O4. It presents as a pale yellow solid and is recognized for its versatile applications across different industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
1-(2,4-dimethoxyphenyl)-2-hydroxyethanone is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its role in this application is attributed to its chemical structure, which allows for further reactions and the creation of a range of medicinal products.
Used in Flavoring and Fragrance Industry:
In the food industry, 1-(2,4-dimethoxyphenyl)-2-hydroxyethanone is utilized as a flavoring agent. Its distinctive properties contribute to enhancing the taste and aroma of various food products, making it a valuable component in the creation of flavors.
Used in Perfumes and Fragrances:
This organic compound is also employed as an ingredient in the perfumery and fragrance industry. Its ability to add unique scents and improve the overall composition of perfumes and fragrances makes it a sought-after component in these products.
Used in Anticancer Research:
1-(2,4-dimethoxyphenyl)-2-hydroxyethanone has been studied for its potential pharmaceutical applications, particularly in the inhibition of the growth of certain cancer cells. Its use in this area is due to its ability to interfere with cellular processes that contribute to cancer progression.
It is crucial to handle 1-(2,4-dimethoxyphenyl)-2-hydroxyethanone with care, as it may cause irritation to the skin, eyes, and respiratory system if not properly managed, highlighting the importance of safety measures during its use in various applications.

Upstream product

• 107-16-4 glycolonitrile 
• 151-10-0 1,3-Dimethoxybenzene 
• 186581-53-3 diazomethane 
• 829-20-9 2',4'-dimethoxyacetophenone 
• 60965-26-6 2-Bromo-2',4'-dimethoxyacetophenone 

Downstream Products

• 91-52-1 2,4 dimethoxybenzoic acid 
• 610770-51-9 (E)-3-(2,3-dimethoxyphenyl)-1-(2'-hydroxy-4',6'-dimethoxyphenyl)prop-2-en-1-one 
• 944447-06-7 (E)-3-(3,5-dimethoxyphenyl)-1-(2'-hydroxy-4',6'-dimethoxyphenyl)prop-2-en-1-one 
• 108979-08-4 (E)-1-(2′-hydroxy-4′,6′-dimethoxyphenyl)-3-(4-bromophenyl)prop-2-en-1-one 
• 861107-96-2 (E)-3-(4-fluorophenyl)-1-(2'-hydroxy-4',6'-dimethoxyphenyl)prop-2-en-1-one 
• 3420-72-2 2'-hydroxy-4,4',6'-trimethoxychalcone 
• 114021-60-2 2'-hydroxy-3,4,4',6'-tetramethoxychalcone 
• 21392-57-4 Dimethyl-chrysin 
• 1610616-99-3 (R)-4-(2,4-dimethoxyphenyl)-4-vinyl-1,3-dioxolane 

Relevant articles and documents

Chiral Bidentate Phosphoramidite-Pd Catalyzed Asymmetric Decarboxylative Dipolar Cycloaddition for Multistereogenic Tetrahydrofurans with Cyclic N-Sulfonyl Ketimine Moieties

An asymmetric [3 + 2] cycloaddition of vinyl ethylenecarbonates (VECs) and (E)-3-arylvinyl substituted benzo[d] isothiazole 1,1-dioxides has been developed using the Pd complex of a bidentate phosphoramidite (Me-BIPAM) as the catalyst, providing a wide variety of chiral multistereogenic vinyltetrahydrofurans in good yields with excellent diastereo- and enantioselectivities (up to >20:1 dr, 99% ee).