62881-59-8

Usage

Usage

Pharmaceutical and agricultural products
Commonly used to control fungal diseases in crops and human or animal infections.

Classification

Triazole antifungals
Belongs to the class of triazole antifungals.

Mode of action

Inhibition of ergosterol synthesis
Works by inhibiting the synthesis of ergosterol, an essential component of the fungal cell membrane.

Structure

Chlorophenyl and triazol-1-yl groups
Consists of a chlorophenyl group and a triazol-1-yl group attached to an ethanol molecule.

Effectiveness

Treating various fungal infections
Has shown effective results in treating various fungal infections.

Value

Asset in agricultural and medical industries
A valuable asset in the agricultural and medical industries.

Upstream product

• 288-88-0 1,2,4-Triazole 
• 6378-66-1 2-chloro-1-(4-chlorophenyl)ethanol 
• 536-38-9 4-chlorobenzoylmethyl bromide 
• 58905-19-4 1-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone 
• 104-88-1 4-chlorobenzaldehyde 
• 103817-03-4 1-<(trimethylsilyl)methyl>-1,2,4-triazole 

Downstream Products

• 62850-93-5 1-[2-allyloxy-2-(4-chloro-phenyl)-ethyl]-1H-[1,2,4]triazole 
• 62843-46-3 1-acetoxy-1-(4-chloro-phenyl)-2-[1,2,4]triazol-1-yl-ethane 
• 157469-27-7 4-[1-(4-chloro-phenyl)-2-[1,2,4]triazol-1-yl-ethoxycarbonylmethyl]-5-oxo-oxazolidine-3-carboxylic acid 2,2,2-trichloro-ethyl ester 

Relevant academic research and scientific papers

Research on antibacterial and antifungal agents. X. Synthesis and antimicrobial activities of 1-phenyl-2-(1H-azol-1-yl) ethane derivatives. Anticonvulsant activity of 1-(4-methylphenyl)-2-(1H-imidazol-1-yl) ethanol.

The synthesis and antimicrobial activity of new phenylazolylethane derivatives are reported.Antimicrobial data in comparison with those obtained with miconazole, fluconazole, enilconazole, imazalil sulfate, pipemidic acid and minocycline showed that tested compounds generally possessed poor or weak activity.Toxicity and anticonvulsant activity of 1-(4-methylphenyl)-2-(1H-imidazol-1-yl)ethanol and structural likeness to Denzimol were also tested.The obtained results showed interesting anticonvulsant activity but only on the supraspinal region. azoles / antifungal / anticonvulsant agent

ALKOXIDE-INDUCED REACTION OF 1-AZOLES WITH IMINES AND CARBONYL COMPOUNDS

t-BuOK-induced reaction of 1--1,2,4-triazole with imines to yield (triazol-1-yl)ethylamines and (triazol-5-yl)methylamines was explored.Also, alkoxide-induced desilylation of 1-azoles in the presence of carb

Fungicidal 1-(2-aryl-2-R-ethyl)-1H-1,2,4-triazoles

Novel compounds of the class of 1-(2-aryl-2-R-ethyl)-1H-1,2,4-triazoles having fungicidal and plant-growth regulating properties.

Heterocyclic triazolylethyl ether compounds and their use as pesticides

Fungicidal compounds of the formula: STR1 wherein R3 is hydrogen, R4 is phenyl optionally substituted with one halogen, and R5 is alkyl having up to 5 carbon atoms, alkenyl having up to 5 carbon atoms, alkynyl having up to