63867-04-9

Basic information

• Product Name: Benzenemethanol, 3-hydroxy-4-methoxy-, a-acetate
• CAS NO: 63867-04-9
• Molecular Formula: C10H12O4
• Molecular Weight: 196.203
• Mol File: 63867-04-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 3-hydroxy-4-methoxy-, a-acetate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 3-hydroxy-4-methoxy-, a-acetate(63867-04-9)
• EPA Substance Registry System: Benzenemethanol, 3-hydroxy-4-methoxy-, a-acetate(63867-04-9)

Safety Data

• Hazardous Substances Data: 63867-04-9(Hazardous Substances Data)

Upstream product

• 4383-06-6 3-hydroxy-4-methoxybenzyl alcohol 
• 141-78-6 ethyl acetate 
• 64-19-7 acetic acid 
• 75-36-5 acetyl chloride 
• 98-88-4 benzoyl chloride 
• 108-05-4 vinyl acetate 
• 63866-99-9 5-acetoxymethyl-2-methoxyphenyl acetate 

Downstream Products

• 1195-09-1 5-methyl-2-methoxyphenol 

Relevant articles and documents

A novel silver nanoparticle embedded mesoporous polyaniline (mPANI/Ag) nanocomposite as a recyclable catalyst in the acylation of amines and alcohols under solvent free conditions

A mesoporous polyaniline/silver (mPANI/Ag) nanocomposite has been prepared using mesoporous organic polymer polyaniline with silver nitrate via radical polymerization of aniline monomer in the presence of hydrochloric acid. The mPANI/Ag nanocomposite has been characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectra (EDX), Fourier transform infrared spectroscopy (FT-IR), and ultraviolet-visible absorption spectra (UV-vis). The XRD patterns indicated that the crystalline phase of Ag is cubic. TEM images show that the Ag nanoparticles are well dispersed in the mesoporous polyaniline matrix. The mPANI/Ag acts as an efficient heterogeneous nanocatalyst in the acylation of substituted amines and alcohols using acetic acid. The catalyst is air-stable, inexpensive, easy to prepare and can be reused several times without a significant decrease in activity and selectivity. This journal is

Microwave-accelerated selective acylation of (hydroxyalkyl)phenols using acid chlorides

Highly selective acylation of the alcoholic hydroxy group can be achieved with (hydroxyalkyl)phenols carrying both alcoholic and phenolic hydroxyls by the use of the most common acylating agents, acid chlorides, under microwave irradiation. Copyright Tayl

Enzyme-catalyzed chemoselective transesterification reactions on hydroxymethylated phenolic compounds

The chemoselective capabilities of porcine pancreatic lipase (PPL) in tetrahydrofuran and Candida rugosa lipase (CRL) in diisopropyl ether have been investigated for selective acetylation and deacetylation of hydroxymethylated phenols and hydroxyaryl alky