50637-28-0

Basic information

• Product Name: (3-(Benzyloxy)-5-Methoxyphenyl)Methanol
• Synonyms: (3-(Benzyloxy)-5-Methoxyphenyl)Methanol
• CAS NO: 50637-28-0
• Molecular Formula: C₁₅H₁₆O₃
• Molecular Weight: 244.28574
• Mol File: 50637-28-0.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3-(Benzyloxy)-5-Methoxyphenyl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3-(Benzyloxy)-5-Methoxyphenyl)Methanol(50637-28-0)
• EPA Substance Registry System: (3-(Benzyloxy)-5-Methoxyphenyl)Methanol(50637-28-0)

Safety Data

• Hazardous Substances Data: 50637-28-0(Hazardous Substances Data)

Usage

General Description

(3-(Benzyloxy)-5-Methoxyphenyl)Methanol, also known as dioxolinone, is a chemical compound with the molecular formula C16H16O3. It is a white solid that is used in organic synthesis and pharmaceutical research. The compound has been studied for its potential therapeutic properties, including as an anti-inflammatory and analgesic agent. It is also a precursor in the synthesis of other biologically active molecules. (3-(Benzyloxy)-5-Methoxyphenyl)Methanol has demonstrated potential as a versatile building block in the development of new drugs and therapeutic agents.

Upstream product

• 50637-25-7 Ethyl-3-benzyloxy-5-methoxybenzoat 
• 50637-26-8 methyl 3-(benzyloxy)-5-methoxybenzoate 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 54915-31-0 methyl 3-(benzyloxy)-5-hydroxybenzoate 
• 100-39-0 benzyl bromide 
• 19520-75-3 3-hydroxy-5-methoxybenzoic acid 
• 19520-74-2 3-hydroxy-5-methoxy-benzoic acid methyl ester 
• 134868-93-2 3-(benzyloxy)-5-(hydroxymethyl)phenol 
• 74-88-4 methyl iodide 
• 99-10-5 3,5-Dihydroxybenzoic acid 

Downstream Products

• 50637-29-1 3-(benzyloxy)-5-methoxybenzaldehyde 
• 58026-13-4 1-(benzyloxy)-3-(bromomethyl)-5-methoxybenzene 
• 97227-86-6 (5-benzyloxy-2-bromo-3-methoxy-phenyl)-methanol 
• 519-57-3 sulochrin 
• 178749-81-0 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzaldehyde 
• 178749-82-1 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzoic acid methyl ester 
• 247086-81-3 (4-benzyloxy-2-hydroxymethyl-6-methoxy-phenyl)-(2,6-bis-benzyloxy-4-methyl-phenyl)-methanone 
• 178749-80-9 2,6-bis-benzyloxy-4-methyl-benzoic acid 5-benzyloxy-2-bromo-3-methoxy-benzyl ester 
• 247086-79-9 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzoic acid 
• 67884-29-1 3,4'-dihydroxy-5-methoxybibenzyl 
• 67884-30-4 5-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxyphenol 
• 70677-47-3 canniprene 
• 83088-28-2 gigantol 
• 42438-89-1 3,4'-dihydroxy-5-methoxystilbene 

Relevant articles and documents

PHENANTHRENE AMPK ACTIVATOR COMPOUNDS, COMPOSITIONS, METHODS AND USES THEREOF

The present invention relates to a compound having general formula I for use in the activation of AMPK. A composition comprising said compound for use in the activation of AMPK is also provided.

AROMATIC RING COMPOUND

Provided is an aromatic ring compound having a GPR40 agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof has a GPR40 agonist activity, and is useful as an agent for the prophylaxis or treatment of diabetes and the like.

Dendrimer disassembly in the gas phase: A cascade fragmentation reaction of frechet dendrons

The mass spectrometry characterization of Frechet-type dendrons is reported. In order to provide the charges necessary for electrospray ionization, dendrons bearing an OH group at the focal point can be deprotonated and observed in the negative ion mode.