110860-92-9

Usage

Uses

Used in Pharmaceutical Industry:
2,3-Dichloro-5-hydroxypyridine is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its reactivity and the presence of functional groups make it a valuable building block in the synthesis of drugs with potential therapeutic applications.
Used in Chemical Industry:
2,3-Dichloro-5-hydroxypyridine is used as a chemical intermediate in the synthesis of complex organic compounds. Its versatility in participating in various chemical reactions allows for the creation of a wide range of products, from specialty chemicals to advanced materials.
Used in Research and Development:
2,3-Dichloro-5-hydroxypyridine is used as a research compound in academic and industrial laboratories. Its unique structure and reactivity make it an interesting subject for studies in organic chemistry, potentially leading to the discovery of new reactions or the development of novel synthetic methods.

InChI:InChI=1/C5H3Cl2NO/c6-4-1-3(9)2-8-5(4)7/h1-2,9H

Upstream product

• 74115-12-1 5-chloropyridin-3-ol 
• 110861-18-2 5-acetoxy-2,3-dichloropyridine 
• 98121-41-6 5-Amino-2,3-dichloropyridine 
• 22353-38-4 3-chloro-2-hydroxy-5-nitropyridine 
• 22353-40-8 2,3-dichloro-5-nitropyridine 
• 5418-51-9 5-nitro-2-hydroxypyridine 

Downstream Products

• 1654021-72-3 ((5,6-dichloro-2-cyanopyridin-3-yl)oxy)acetic acid ethyl ester 

Relevant academic research and scientific papers

PESTICIDALLY ACTIVE TETRACYCLIC DERIVATIVES WITH SULFUR CONTAINING SUBSTITUENTS

Compounds of formula (I) wherein the substituents are as defined in claim 1, and the agrochemically acceptable salts, stereoisomers, enantiomers, tautomers and N-oxides of those compounds, can be used as insecticides and can be prepared in a manner known per se.

N-SUBSTITUTED BENZAMIDES AND METHODS OF USE THEREOF

The invention provides novel compounds having the general formula: [insert formula (I)] and pharmaceutically acceptable salts thereof, wherein the variables RA, subscript n, ring A, X2, L, subscript m, X1, ring D, R1, and RN have the meaning as described

Multi-gram synthesis of a nucleotide-competing reverse transcriptase inhibitor

An efficient multi-gram synthesis of a nucleotide-competing reverse transcriptase inhibitor is reported. The synthesis features a chiral auxiliary-assisted alcohol resolution, a Mitsunobu reaction involving a carbamate, followed by a lithium-iodide exchange/Weinreb ketone synthesis tandem. These chemical transformations were optimized in order to increase the yield of the synthesis. The route is concluded by a late-stage palladium-catalyzed cyanation followed by a pyrimidine-2-one ring formation.

Substituted 2-phenylpyridines as herbicides

2-Phenylpyridines I an their salts, wherein R1to R17, X1-X3are as defined in the specification. The compounds are useful as herbicides, desiccants and defoliants.

3-Pyridyl enantiomers and their use as analgesics

The present invention relates to a method of controlling pain in mammals, including humans, comprising administering to a mammal or patient in need of treatment thereof selected compounds of formula I: STR1 or a pharmaceutically acceptable salt thereof. The invention further relates to selected (R) and (S) compounds of formula I above which are useful as analgesics as well as neuronal cell death preventors and anti-inflammatories.

Pyridine derivatives and the N-oxides thereof, and the use thereof as intermediates for the synthesis of plant protecting agents

The compounds of the formula I STR1 in which A denotes N or N→O, Z denotes O or NH, R denotes H, (halo)alkyl, (halo)alkenyl, (halo)alkynyl or alkoxycarbonyl, R1 denotes hydrogen, halogen, amino, --NHOH, hydroxyl, (substituted) phenylazo or a ra