63277-46-3

Usage

Category

Chemical compound, specifically an organic compound.

Functionality

Pesticide and acaricide, used to control pests and mites.

Mechanism of action

Interferes with the insect's nervous system, leading to paralysis and death.

Usage

Widely used in agriculture to protect crops and in domestic settings for controlling pests.

Precautions

Can be harmful to humans and non-target organisms if not handled and applied properly.

Upstream product

• 29448-81-5 1,3-dihydro-2H-imidazo[4,5-b]pyridine-2-thione 
• 74-88-4 methyl iodide 
• 452-58-4 2,3-Diaminopyridine 
• 29448-81-5 2-mercapto-1H-imidazo[4,5-b]pyridine 

Downstream Products

• 1357143-01-1 2-(4-bromophenoxy)-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridine 
• 1357143-02-2 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-3-{[2-(trimethylsilyl)ethoxy]methyl}-3H-imidazo[4,5-b]pyridine 
• 1357143-33-9 2-(4-bromophenoxy)-3-(2-methoxyethyl)-3H-imidazo[4,5-b]pyridine 
• 1357143-47-5 2-(4-bromophenoxy)-3-(2,2-difluoroethyl)-3H-imidazo[4,5-b]pyridine 

Relevant academic research and scientific papers

INHIBITORS OF HIV-1 NEF FOR THE TREATMENT OF HIV DISEASE

A compound of formula I, or a stereoisomer, tautomer, or pharmaceutically acceptable salt thereof: Formula I wherein X1 is benzimidazolyl, substituted benzimidazolyl, azabenzimidazolyl, substituted azabenzimidazolyl, pyrazolyl, or substituted pyrazolyl; X2 is aryl, substituted aryl, arylalkyl, substituted arylalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, cycloalkyl, substituted cycloalkyl, (cycloalkyl)alkyl, substituted (cycloalkyl)alkyl, heterocycloalkyl, substituted heterocycloalkyl, (heterocycloalkyl)alkyl, substituted (heterocycloalkyl)alkyl, alkyl, substituted alkyl, alkoxycarbonyl, substituted alkoxycarbonyl, dialkylaminocarbonyl, substituted dialkylaminocarbonyl, (heterocycloalkyl)carbonyl, or substituted (heterocycloalkyl)carbonyl; X3 is alkyl, substituted alkyl, alkenyl, substituted alkenyl, heterocycloalkyl, substituted heterocycloalkyl, (heterocycloalkyl)alkyl, substituted (heterocycloalkyl)alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, cycloalkyl, substituted cycloalkyl, (cycloalkyl)alkyl, or substituted (cycloalkyl)alkyl; and X4 is hydroxy, amino, alkyl, or hydrogen.

FUSED HETEROCYCLIC COMPOUNDS

The present invention provides a compound which has the effect of PDE 10A inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound represented by the formula (1'): wherein, Ring A' represents an optiona

An alternative total synthesis of pentosidine

Pentosidine, a fluorescent advanced glycation endproduct that serves as a biomarker of diabetic complications, kidney dysfunction, oxidative stress, and aging and age-related diseases, was synthesized from 2,3-diaminopyridine and benzyloxycarbonyl (Cbz) p

FUSED HETEROCYCLIC COMPOUNDS

The present invention provides a compound which has the effect of PDE inhibition, and which is useful as an agent for preventing or treating schizophrenia. The compound is represented by the formula (I): wherein the symbols are defined in the specification.

A straightforward synthesis of pentosidine framework

This work was performed under Professor Sayre's direction. Professor Lawrence M. Sayre passed away May 8, 2009, following an incapacitating stroke. His impact on the lives of his colleagues, students, and friends was profound and he is deeply missed [3]. We dedicate this article to him as a great mentor and brilliant scientist. (Chemical Equation Presented) Pentosidine framework 4-butyl-2-propyl-4H-aminoimidazo[4,5-b]pyridine (2) was synthesized through a five steps reaction sequence. The regiochemistry of 2 was confirmed by an unambiguous synthesis, and the UV absorption and fluorescent properties of 2 were examined.