157953-16-7

Basic information

• Product Name: 1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone
• Synonyms: 1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone
• CAS NO: 157953-16-7
• Molecular Weight: 458.296
• Mol File: 157953-16-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone(157953-16-7)
• EPA Substance Registry System: 1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone(157953-16-7)

Safety Data

• Hazardous Substances Data: 157953-16-7(Hazardous Substances Data)

Usage

Description

1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone is a chemical compound characterized by the presence of two benzyl ether groups and an iodine atom on a phenyl ring, which is attached to an ethanone (or ketone) functional group. 1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone is recognized for its unique reactivity due to the iodine atom and is frequently employed as an intermediate in organic synthesis.

Uses

Used in Pharmaceutical Industry:
1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone is used as a chemical intermediate for the production of various pharmaceuticals. Its unique reactivity and structural features make it a valuable building block in the synthesis of diverse medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone is utilized as a precursor in the synthesis of different agrochemicals. Its versatility allows for the creation of compounds with specific pesticidal or herbicidal properties.
Used in Organic Synthesis:
1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone is used as a versatile building block in organic synthesis. The presence of the iodine atom provides additional reactivity, enabling a wide range of chemical reactions and transformations, which are of interest to researchers and chemists in various fields.
Used in Research and Development:
1-(2,4-Bis(benzyloxy)-5-iodophenyl)ethanone is also used in research and development settings, where its unique properties are explored for potential applications in creating new materials, improving existing synthesis methods, and discovering novel chemical reactions.

Upstream product

• 22877-01-6 2,4-bis(benzyloxy)acetophenone 

Downstream Products

• 157953-23-6 1-[2,4-Bis-benzyloxy-5-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-ethanone 
• 62069-33-4 1-(2,4-dihydroxy-5-iodophenyl)ethanone 
• 19013-03-7 6-acetyl-7-hydroxy-2,2-dimethyl-1H-chromene 
• 532-48-9 1-(6-hydroxy-2-isopropenyl-benzofuran-5-yl)-ethanone 
• 173992-05-7 5-acetyl-6-hydroxy-2-(1-hydroxy-1-methylethyl)benzofuran 
• 173992-03-5 5'-iodo-2',4'-bis(tosyloxy)acetophenone 
• 173992-04-6 5'-(3-hydroxy-3-methylbutynyl)-2',4'-bis(tosyloxy)acetophenone 
• 28437-37-8 5-C-prenylresacetophenone 
• 1026247-18-6 1-[2,4-Dihydroxy-5-(3-hydroxy-3-methyl-butyl)-phenyl]-ethanone 
• 157953-27-0 C₂₇H₂₄O₅ 

Relevant articles and documents

REGIOSELECTIVE PRENYLATION OF PHENOLS BY PALLADIUM CATALYST: SYNTHESES OF PRENYLPHENOLS AND CHROMANS

The palladium-catalyzed coupling reaction of iodophenols (1) with 2-methyl-3-butyn-2-ol gave alkynylphenols (2).Catalytic hydrogenation of 2 over Raney nickel and the subsequent dehydration of the resultant alkylphenols (3) gave regioselectively the desired prenylphenols (4).Dehydration of alkylphenols (3f-h) gave chromans (7).