21022-74-2

Basic information

• Product Name: 6-Isopropyl-2-MethoxyPhenol
• Synonyms: 6-Isopropyl-2-MethoxyPhenol
• CAS NO: 21022-74-2
• Molecular Formula: C₁₀H₁₄O₂
• Molecular Weight: 166.21696
• Mol File: 21022-74-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-Isopropyl-2-MethoxyPhenol(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Isopropyl-2-MethoxyPhenol(21022-74-2)
• EPA Substance Registry System: 6-Isopropyl-2-MethoxyPhenol(21022-74-2)

Safety Data

• Hazardous Substances Data: 21022-74-2(Hazardous Substances Data)

Usage

General Description

6-Isopropyl-2-MethoxyPhenol, also known as propofol, is a chemical compound commonly used as an intravenous anesthetic. It belongs to the class of phenols and is derived from guaiacol, an organic compound. Propofol is a colorless liquid with a slightly phenolic odor and is often administered intravenously for the induction and maintenance of anesthesia during surgery or other procedures. It acts as a sedative-hypnotic agent, producing anesthesia by disrupting the activity of neurotransmitter receptors in the brain. Propofol is considered to have a rapid onset and short duration of action, making it a popular choice for anesthesia in medical settings.

Upstream product

• 87307-81-1 3-methoxy-2-hydroxy-α-methylstyrene 
• 90-05-1 2-methoxy-phenol 
• 67-63-0 isopropyl alcohol 
• 2138-48-9 3-isopropylbenzene-1,2-diol 
• 77-78-1 dimethyl sulfate 
• 917-64-6 methyl magnesium iodide 
• 1728-86-5 2-bromo-7-methoxytropone 
• 21022-77-5 2-Chlor-7-methoxy-tropon 
• 21022-76-4 2-(2-hydroxy-3-methoxy-phenyl)-propan-2-ol 
• 914454-83-4 2-benzyloxy-3-i-propylanisole 
• 6342-70-7 3-methoxymethylsalicylate 

Downstream Products

• 133393-99-4 1-(4-hydroxy-3-isopropyl-5-methoxy-phenyl)-ethanone 
• 173059-60-4 2-acetoxy-1-isopropyl-3-methoxy-benzene 
• 71720-27-9 3-Isopropyl-veratrol 
• 83569-73-7 1-methoxy-2-allyloxy-3-isopropylbenzene 
• 2138-48-9 3-isopropylbenzene-1,2-diol 
• 177990-70-4 2-(2-isopropyl-6-methoxyphenoxy)acetic acid 
• 914454-89-0 2-(2-i-propyl-6-methoxyphenoxy)-1-bromoethane 
• 914455-01-9 2-(2-i-propyl-6-methoxyphenoxy)ethylamine 
• 914454-93-6 2-(2-i-propyl-6-methoxyphenoxy)ethylazide 
• 83569-74-8 1-methoxy-2-hydroxy-3-isopropyl-5-allylbenzene 
• 83569-75-9 1,2-dimethoxy-3-isopropyl-5-allylbenzene 
• 83569-70-4 3-(3,4-dimethoxy-5-isopropylphenyl)propanol 
• 83569-76-0 3-(3,4-dimethoxy-5-isopropylphenyl)propanal 
• 83569-77-1 2-methyl-5-(3,4-dimethoxy-5-isopropylphenyl)-1-penten-3-ol 

Relevant articles and documents

Zirconia-modified superacid UDCaT-5: An efficient and versatile catalyst for alkylation reactions under solvent-free conditions

UDCaT-5, a modified version of zirconia, efficiently catalyzes alkylation of phenols with alcohols under environmentally safe, heterogeneous reaction conditions with high selectivity and in excellent yields. The high content present in UDCaT-5 with preservation of tetragonal phase of zirconia was responsible for the superactivity. Several phenolic compounds carrying either electron-sulfer releasing or electron-withdrawing substituents in the ortho, meta, and para positions afforded high yields of the products. Copyright Taylor & Francis Group, LLC.

AN APPROACH TO TAXODIONE INVOLVING BIOMIMETIC POLYENE CYCLIZATION METHODOLOGY

A novel synthesis of 11,12-dimethoxyabieta-8,11,13-triene (4), involving the biomimetic cyclization of allylic alcohol 5 is described.This represents a formal total synthesis of taxodione (1), a tumor-inhibitory diterpenoid quinone methide.Treatment of th