64490-45-5

Usage

Uses

Used in Organic Synthesis:
(2-iodo-3,4,5-trimethoxyphenyl)methanol is used as a building block for the synthesis of various biologically active molecules. Its unique structure and functional groups make it a versatile compound for creating new organic molecules with potential applications in various fields.
Used in Medicinal Chemistry:
(2-iodo-3,4,5-trimethoxyphenyl)methanol is used as a key intermediate in the preparation of pharmaceuticals. Its iodine and methoxy groups can be utilized to introduce specific functional groups into drug molecules, potentially enhancing their therapeutic properties and effectiveness.
Used in Agrochemicals:
(2-iodo-3,4,5-trimethoxyphenyl)methanol is also used in the development of agrochemicals. Its functional groups can be incorporated into molecules designed to protect crops and enhance agricultural productivity.
Used in Chemical Research:
(2-iodo-3,4,5-trimethoxyphenyl)methanol serves as a valuable tool for chemical research, particularly in the study of functional group introduction and the development of new synthetic methods. Its unique properties make it an interesting subject for exploration and potential innovation in the field of chemistry.

Upstream product

• 665004-29-5 6,6'-bis(2-iodo-3,4,5-trimethoxybenzyl 1,3-benzodioxole-5-carboxylate) 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 73252-53-6 3,4,5-trimethoxy-2-iodobenzaldehyde 

Downstream Products

• 64490-46-6 2-Iodo-3,4,5-trimethoxybenzyl chloride 
• 73252-53-6 3,4,5-trimethoxy-2-iodobenzaldehyde 
• 117370-33-9 2-<2-(trimethylsilyl)ethynyl>-3,4,5-trimethoxybenzenemethanol 
• 117370-31-7 (E)-3,4,5-trimethoxy-2-<2-(trimethylsilyl)ethenyl>benzenemethanol 
• 258283-81-7 6-(6-hydroxymethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole-5-carbaldehyde 
• 293732-22-6 1-(bromomethyl)-2-iodo-3,4,5-trimethoxybenzene 
• 638164-09-7 2-iodo-3,4,5-trimethoxy-1-(2-methoxy-ethoxymethoxymethyl)-benzene 
• 638164-08-6 1-iodo-6-triethylsilyloxymethyl-2,3,4-trimethoxybenzene 
• 638164-07-5 2-iodo-3,4,5-trimethoxy-1-methoxymethoxymethyl-benzene 
• 665004-27-3 2-iodo-3,4,5-trimethoxybenzyl 6-iodo-1,3-benzodioxole-5-carboxylate 
• 891194-33-5 C₁₄H₁₈INO₇ 
• 665004-28-4 6-iodo-1,3-benzodioxol-5-ylmethyl 2-iodo-3,4,5-trimethoxybenzoate 
• 851384-86-6 [1-(2-iodo-3,4,5-trimethoxy-benzyl)-1H-pyrrol-2-yl]-morpholin-4-yl-methanone 
• 293732-40-8 1-(2-iodo-3,4,5-trimethoxybenzyl)pyrrole-2-carboxylic acid diethyl amide 

Relevant academic research and scientific papers

Pd-catalyzed atom-efficient cross-coupling of triarylbismuth reagents with protecting group-free iodophenylmethanols: Synthesis of biarylmethanols

An atom-efficient procedure for the synthesis of functionalized biarylmethanols via the Pd-catalyzed cross-coupling reactions of differently functionalized iodophenylmethanols and triarylbismuth reagents is described. This protecting group-free direct couplings of 2-, 3- or 4-iodophenylmethanols with triarylbismuth reagents afforded biarylmethanols in good to high yields.

Intramolecular biaryl coupling reaction of benzyl benzoate and phenyl benzoate derivatives, and its application to the formal synthesis of (-)-steganone

Construction of the biaryl moiety of stegane and related compounds through an intramolecular biaryl coupling reaction is described. Undesired products were obtained by the intramolecular coupling reaction of benzyl benzoates (8, 13, and 14) because of the

An attempt for biaryl coupling reaction of benzyl benzoate derivatives under Ullmann conditions

The biaryl coupling reaction of benzyl benzoate derivatives (3) and (4) was examined with copper(0) reagent. A dimerized product (9) was mainly obtained whereas the desired intramolecularly coupled product (11) was not detected when 3 was employed as the

A concise approach towards the synthesis of steganone analogues

The cobalt-mediated [2+2+2] cycloaddition of a tethered deca-1,9-diyne is used as a key step in a highly convergent route to steganone analogues.