99179-72-3

Usage

Uses

Used in Organic Synthesis:
4-Methoxy-1,3-benzenediol 3-Acetate is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to be a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. The presence of the methoxy and acetate groups makes it a valuable precursor for the development of new molecules with potential biological activities or improved properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methoxy-1,3-benzenediol 3-Acetate is used as a key intermediate in the synthesis of drugs with therapeutic potential. Its chemical properties enable the creation of novel drug candidates that can target specific biological pathways or receptors, leading to the development of more effective treatments for various diseases and conditions.
Used in Agrochemical Industry:
4-Methoxy-1,3-benzenediol 3-Acetate also finds application in the agrochemical industry, where it serves as a starting material for the synthesis of pesticides, herbicides, and other crop protection agents. Its unique structure allows for the development of new compounds with improved efficacy, selectivity, and environmental compatibility.
Used in Specialty Chemicals:
In the specialty chemicals sector, 4-Methoxy-1,3-benzenediol 3-Acetate is utilized in the production of various high-value compounds, such as dyes, pigments, and fragrances. Its chemical properties make it suitable for the development of new specialty chemicals with unique properties and applications, catering to the needs of diverse industries.

Upstream product

• 621-59-0 isovanillin 
• 108-24-7 acetic anhydride 
• 881-57-2 isovanillin acetate 

Downstream Products

• 7298-21-7 1-(2,4-dihydroxy-5-methoxyphenyl)ethan-1-one 
• 1415914-34-9 (E)-3-(dimethylamino)-1-(2-hydroxy-5-methoxy-4-(tetrahydro-2H-pyran-2-yloxy)phenyl)prop-2-en-1-one 
• 1252801-60-7 1-(2-hydroxy-5-methoxy-4-(tetrahydro-2H-pyran-2-yloxy)phenyl)ethanone 
• 103203-40-3 (4-hydroxy-2,5-dimethoxy-phenyl)-glyoxylic acid 
• 18113-18-3 2,5-dimethoxyphenol 
• 27257-06-3 2,5-dimethoxyphenyl acetate 
• 6100-60-3 4-methoxybenzene-1,3-diol 

Relevant academic research and scientific papers

SYNTHESIS OF 13C-LABELLED ESTROGEN ANALOGUES

There is provided a method of producing novel 13C-labelled estrogen analogues. The method preferably proceeds via an intermediate A or B or which is a mixture of (A) or (B): wherein a13C atom is located at one or more of positions 1, 2, 3 or 4 and wherein R is an optionally substituted alkane, alkene, alkyne or aryl group. Preferably R is -CH2Ph. An alternative preferred intermediate compound is 13C-resorcinol.

The synthesis of [2,3,4-13C3]glycitein

Glycitein is one of the soy isoflavones which have attracted considerable interest in recent years due to their possible beneficial effects on human health. However, glycitein has been much less studied than other members of this family due to the lack of

Mechanistic Studies of Selective Catechol Formation from o-Methoxyphenols using a Copper(II)-Ascorbic Acid-Dioxygen System

Mechanistic details of selective conversion of o-methoxyphenols to the corresponding catechols using a Cu2+-ascorbic acid-O2 system, were studied. 2,5-Dimethoxyphenol was converted predominantly to the o-demethylated compound and partially to the m-demethylated one.Anisole with no phenolic hydroxy group was much less reactive.When guaiacol (1). guaiacol and 2-methoxy-6-methoxyphenol was used as substrates, moderate intermolecular and intramolecular kinetic isotope effects were observed (1.4-1.9). Catechol was derived from 1 in nine-fold excess over catechol when the reaction was run in an 18O2 atmosphere with natural water as a solvent, though no catechol was formed when using natural O2 and H218O.It was determined that the Cu2+-ascorbic acid-O2 system operates in a monooxygenase mode because the oxygen atom of dioxygen (not water) was incorporated into the products, and this oxidative conversion proceeded mainly via ipso-substitution at the methoxy position, probably with hydroxyl radical coordinated to the cupric ion as the active oxygen species.