850146-80-4

Usage

Uses

Used in Organic Synthesis:
Methyl 2-hydroxy-5-iodo-4-methylbenzoate is used as an intermediate in the synthesis of various organic compounds. Its unique structural features allow for versatile chemical reactions, making it a valuable building block in the development of new molecules.
Used in Pharmaceutical Research:
Methyl 2-hydroxy-5-iodo-4-methylbenzoate is used as a starting material in the development of new pharmaceutical agents. Its reactivity and structural features can be exploited to create novel drug candidates with potential therapeutic applications.
Used in Laboratory Settings:
Methyl 2-hydroxy-5-iodo-4-methylbenzoate is used as a research compound in laboratory settings. It is important to handle methyl 2-hydroxy-5-iodo-4-methylbenzoate with caution and follow proper safety protocols to ensure the safety of researchers and the integrity of experiments.

Upstream product

• 4670-56-8 methyl 2-hydroxy-4-methylbenzoate 
• 850146-83-7 2-hydroxy-5-iodo-4-methylbenzoic acid 
• 74-88-4 methyl iodide 

Relevant academic research and scientific papers

Total Synthesis of (±)-Phaeocaulisin D

The tropone sesquiterpene phaeocaulisin D, isolated from the rhizomes of Curcuma phaeocaulis, has previously been shown to inhibit nitric oxide production in macrophages. A total synthesis of phaeocaulisin D was accomplished by using an intramolecular cyc

PROCESS FOR PREPARING ALKYNYL-CONTAINING COMPOUND AND INTERMEDIATE THEREOF

Disclosed are processes for preparing alkylnyl-containing compounds of Formula (I) as shown below, intermediates and related compounds thereof. Pharmaceutical compositions comprising the compounds and methods of treating cancer thereof are also disclosed.

APOPTOSIS SIGNAL-REGULATING KINASE INHIBITORS AND USES THEREOF

Described herein are ASK1 inhibitors and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful for the treatment of blood disease, autoimmune disorders, pulmonary disorders, hypertension, inflammatory diseases, fibrotic diseases, diabetes, diabetic nephropathy, renal diseases, respiratory diseases, cardiovascular diseases, acute lung injuries, acute or chronic liver diseases, and neurodegenerative diseases.

A simple and effective method for chemoselective esterification of phenolic acids

A new method for efficient and chemoselective esterification of phenolic acids in KHCO3/alkyl halide/DMF reaction system is described, by which a series of phenoic acid esters were obtained in excellent yields.