677299-16-0

Usage

Uses

Used in Pharmaceutical Industry:
(2R,3R,4R)-3,4-bis((2,4-dichlorobenzyl)oxy)-2-(((2,4-dichlorobenzyl)oxy)methyl)-5-methoxytetrahydrofuran is used as a potential pharmaceutical agent for its complex molecular structure that may exhibit bioactivity. The presence of dichlorobenzyl and methoxy groups could allow it to interact with biological targets, making it a candidate for further research into drug development.
Used in Agrochemical Industry:
In the agrochemical field, (2R,3R,4R)-3,4-bis((2,4-dichlorobenzyl)oxy)-2-(((2,4-dichlorobenzyl)oxy)methyl)-5-methoxytetrahydrofuran may serve as a precursor or intermediate in the synthesis of bioactive compounds for pest control or crop protection. Its structural elements could be key in the development of new agrochemicals with specific modes of action.
Further research would be essential to explore and validate the specific properties and uses of (2R,3R,4R)-3,4-bis((2,4-dichlorobenzyl)oxy)-2-(((2,4-dichlorobenzyl)oxy)methyl)-5-methoxytetrahydrofuran, as its complex nature suggests a range of potential applications contingent upon its reactivity, stability, and interaction with biological systems.

Upstream product

• 1824-96-0 methyl ribofuranoside 
• 94-99-5 2,4-Dichlorobenzyl chloride 

Downstream Products

• 168427-35-8 (3R,4S,5R)-4-((2,4-dichlorobenzyl)oxy)-5-(((2,4-dichlorobenzyl)oxy)methyl)-2-methoxytetrahydrofuran-3-ol 
• 636581-81-2 3,5-bis-O-(2,4-dichlorobenzyl)-1-O-methyl-α-D-ribofuranose 
• 875302-64-0 1-bromo-2,3,5-tri-O-(2,4-dichlorobenzyl)-D-ribose 
• 1496552-16-9 C₂₂H₂₉FN₃O₉P 
• 443642-30-6 3,5-bis-O-(2,4-dichlorophenylmethyl)-1-O-methyl-α-D-erythro-pentafuranos-2-ulose 
• 443642-31-7 (2S,3R,4R,5R)-4-((2,4-dichlorobenzyl)oxy)-5-(((2,4-dichlorobenzyl)oxy)methyl)-2-methoxy-3-methyltetrahydrofuran-3-ol 
• 1394157-34-6 C₂₀H₂₅FN₃O₉P 
• 2164516-85-0 C₂₁H₂₇FN₃O₉P 
• 1496552-16-9 C₂₂H₂₉FN₃O₉P 

Relevant academic research and scientific papers

RNAI INHIBITION OF INFLUENZA VIRUS REPLICATION

The invention relates to compositions and methods for modulating the expression of influenza viral genes, and more particularly to the downregulation of influenza viral genes by chemically modified oligonucleotides

Efficient synthesis of methyl 3,5-di-O-benzyl-α-D-ribofuranoside and application to the synthesis of 2′-C-β-alkoxymethyluridines

Methyl 3,5-di-O-arylmethyl-α-D-ribofuranosides have been used extensively as synthons to construct 2'-C-branched ribonucleosides. Herein, we describe efficient access to methyl 3,5-di-O-arylmethyl-α-D- ribofuranosides (aryl: 2-ClC6H4, 3-ClC6H 4, 4-ClC6H4, 4-BrC6H4, 2,4-Cl2C6H3, Ph) in 72-82% yields from methyl D-ribofuranoside. We also demonstrate efficient access to the versatile precursor methyl 3,5-di-O-benzyl-α-D-ribofuranoside (3f) and the synthesis of 2′-C-β-methoxymethyl- and 2′-C-β-ethoxymethyluridine in six steps from 3f with overall yields of 18% and 32%, respectively.