62536-85-0

Basic information

• Product Name: 2-formyl-4-methoxyphenyl acetate
• CAS NO: 62536-85-0
• Molecular Formula: C₁₀H₁₀O₄
• Molecular Weight: 194.184
• Mol File: 62536-85-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 327°C at 760 mmHg
• Flash Point: 145.4°C
• Density: 1.193g/cm³
• Vapor Pressure: 0.000208mmHg at 25°C
• Refractive Index: 1.539
• CAS DataBase Reference: 2-formyl-4-methoxyphenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-formyl-4-methoxyphenyl acetate(62536-85-0)
• EPA Substance Registry System: 2-formyl-4-methoxyphenyl acetate(62536-85-0)

Safety Data

• Hazardous Substances Data: 62536-85-0(Hazardous Substances Data)

Upstream product

• 672-13-9 2-hydroxy-5-methoxybenzaldehyde 
• 108-24-7 acetic anhydride 
• 108-22-5 Isopropenyl acetate 

Downstream Products

• 33538-96-4 5-Methoxy-2-acetoxyzimtaldehyd 
• 672-13-9 2-hydroxy-5-methoxybenzaldehyde 
• 64-19-7 acetic acid 
• 1092064-21-5 2-(acetoxymethyl)-4-methoxyphenol 
• 63272-65-1 2-Acetoxy-4-bromo-5-methoxybenzaldehyde 
• 115061-31-9 methyl 4,8-diacetoxy-5-methoxynaphthalene-2-carboxylate 
• 115061-30-8 2-[1-(2-Acetoxy-5-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 1-methyl ester 
• 17372-53-1 6-methoxycoumarin 
• 73220-24-3 ethyl (E)-3-(2-hydroxy-5-methoxyphenyl)propenoate 
• 138116-12-8 3-(Diphenyl-phosphinoyl)-6-methoxy-chromen-2-one 
• 2612-02-4 5-methoxysalicylic acid 
• 33538-99-7 2-hydroxy-5-methoxycinnamaldehyde 

Relevant articles and documents

The studies on chemoselective promiscuous activity of hydrolases on acylals transformations

Chemoselective, mild and convenient protocol for the hydrolysis of the synthetically relevant acylals via promiscuous enzyme-catalyzed hydrolysis has been developed. It has been shown that promiscuous activity of the used hydrolases dominates their native activity related with carboxylic esters hydrolysis. The main advantage of the present methodology is that it can be conducted under neutral conditions at room temperature. Moreover, complete deprotection of acylals takes place within 10–20 min. Developed protocol can be used with compounds having a variety of hydrolytic labile groups since the cleavage is proceeded under neutral conditions and occurs exclusively on acylal moiety. Further this protocol was extended by the tandem Passerini multicomponent reaction leading to the α-acetoxy amides using acylals as the surrogates of the carbonyl components to P-MCR.

Molecular iodine in isopropenyl acetate (IPA): a highly efficient catalyst for the acetylation of alcohols, amines and phenols under solvent free conditions

Iodine in isopropenyl acetate (IPA) is a highly efficient catalyst for the acetylation of a variety of alcohols, phenols and amines under solvent free conditions. Primary, secondary, tertiary alcohols, amines and mono to polyhydroxy phenols and anilines with electron donating or withdrawing substituents can be easily acetylated in good to excellent yield at 85-90 °C.

Non-steroid progesterone receptor agonist and antagonist and compounds and methods

Non-steroidal compounds which are high affinity, high specificity ligands for progesterone receptors are disclosed. The compounds include synthetic derivatives of cyclocymopol and its diastereomers, spectroscopically and chromatographically pure (3R)-cyclocymopol monomethyl ether, which functions as a progesterone receptor antagonist, and spectroscopically and chromatographically pure (3S)-cyclocymopol monomethyl ether, which functions as a progesterone receptor agonist. Also disclosed are methods for employing the disclosed compounds for modulating processes mediated by progesterone receptors and for treating patients requiring progesterone receptor agonist or antagonist therapy.