289471-92-7

Basic information

• Product Name: 4-Iodo-2-(phenylMethoxy)phenol
• Synonyms: 2-Benzyloxy-4-iodophenol;4-Iodo-2-(phenylMethoxy)phenol
• CAS NO: 289471-92-7
• Molecular Formula: C₁₃H₁₁IO₂
• Molecular Weight: 326.12971
• Product Categories: Aromatics, Intermediates
• Mol File: 289471-92-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Iodo-2-(phenylMethoxy)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Iodo-2-(phenylMethoxy)phenol(289471-92-7)
• EPA Substance Registry System: 4-Iodo-2-(phenylMethoxy)phenol(289471-92-7)

Safety Data

• Hazardous Substances Data: 289471-92-7(Hazardous Substances Data)

Usage

Description

4-Iodo-2-(phenylMethoxy)phenol is an organic compound characterized by its unique molecular structure, which features an iodine atom at the 4-position and a phenylmethoxy group at the 2-position. 4-Iodo-2-(phenylMethoxy)phenol is known for its potential applications in various fields due to its distinct chemical properties.

Uses

Used in Pharmaceutical Industry:
4-Iodo-2-(phenylMethoxy)phenol is used as an intermediate in the synthesis of isotope-labeled compounds, specifically for the preparation of isotope-labeled Quercetin (Q509500) conjugates. This application is significant in the development of new drugs and the study of biological processes, as isotope labeling allows for the tracking and analysis of these compounds within biological systems.
Used in Chemical Research:
4-Iodo-2-(phenylMethoxy)phenol can also be utilized in chemical research as a starting material for the synthesis of various complex organic molecules. Its unique structure makes it a valuable building block for the creation of novel compounds with potential applications in different industries, such as pharmaceuticals, agrochemicals, and materials science.

Upstream product

• 120-80-9 benzene-1,2-diol 
• 100-44-7 benzyl chloride 
• 6272-38-4 O-benzylcatechol 

Downstream Products

• 872410-34-9 2'-benzyloxy-4-hexyloxy-4''-hexadecyloxy-p-terphenyl 
• 872410-35-0 2'-benzyloxy-4-hexadecyloxy-4''-hexyloxy-p-terphenyl 
• 872410-25-8 3-benzyloxy-4,4''-didecyloxy-p-terphenyl 
• 872410-33-8 3-benzyloxy-4'-hexadecyloxybiphenyl-4-yl trifluoromethanesulfonate 
• 872410-31-6 3-benzyloxy-4'-hexadecyloxybiphenyl-4-ol 
• 872410-32-7 3-benzyloxy-4'-hexyloxybiphenyl-4-yl trifluoromethanesulfonate 
• 872410-30-5 3-benzyloxy-4'-hexyloxybiphenyl-4-ol 
• 289471-95-0 1-iodo-3-benzyloxy-4-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyloxy)benzene 
• 122769-75-9 (S)-benzyl 3-(3-(benzyloxy)-4-hydroxyphenyl)-2-(((benzyloxy)carbonyl)amino)propanoate 
• 872410-29-2 2-benzyloxy-4-iodophenyl acetate 
• 872410-24-7 1-benzyloxy-2-decyloxy-5-iodobenzene 

Relevant articles and documents

CARBIDOPA AND L-DOPA PRODRUGS AND THEIR USE TO TREAT PARKINSON'S DISEASE

The present disclosure relates to (a) carbidopa prodrugs, (b) pharmaceutical combinations and compositions comprising a carbidopa prodrug and/or an L-dopa prodrug, and (c) methods of treating Parkinson's disease and associated conditions comprising administering a carbidopa prodrug and an L-dopa prodrug to a subject with Parkinson's disease.

Isotopic labelling of Quercetin 4'-O-β-D-glucoside

[2-13C]-Quercetin-4'-O-β-glucoside was synthesised in four steps and 28% yield from barium [13C]-carbonate. This short route will be applicable to the synthesis of radiolabelled quercetin-4'-O-β-D-glucoside from barium [14