338418-54-5

Usage

Molecular structure

A heterocyclic organic compound consisting of a benzimidazole ring attached to a 1,2,4-triazole ring through a methyl group.

Common uses

Frequently utilized in pharmaceutical and agricultural applications.

Antimicrobial properties

Exhibits the ability to inhibit or destroy microorganisms, such as bacteria and viruses.

Antifungal properties

Demonstrates the capability to prevent the growth and development of fungi, which can cause infections and diseases.

Antiparasitic properties

Shows the potential to combat parasitic infections by either killing parasites or inhibiting their growth.

Treatment of infectious diseases

Has been studied for its potential use in treating various infectious diseases caused by microorganisms.

Fungicide

Evaluated for its role in inhibiting the growth and development of plant pathogens, making it a valuable component in the agricultural industry.

Pest control

Assessed for its effectiveness in controlling pests that affect crops and other plants.

Upstream product

• 28711-29-7 2-(1H-1,2,4-triazol-1-yl)acetic acid 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 1417605-69-6 C₁₉H₁₇N₅O₂ 
• 1417605-73-2 C₂₀H₁₉N₅O₂ 
• 1403683-05-5 {[Cd(1,3-benzenedicarboxylate)(2-((1H-1,2,4-triazol-1-yl)methyl)-1H-benzimidazole)(H₂O)]*CH₃OH}n 

Relevant academic research and scientific papers

Synthesis, crystal structure, photoluminescent, and electrochemical properties of a novel 2-D silver(I) coordination polymer with 1H-1,2,4-triazole-1-methylene-1H-benzimidazole-1-acetic acid

A new Ag(I) complex [AgL]n (HL = 1H-1,2,4-triazole-1-methylene- 1H-benzimidazole-1-acetic acid) was synthesized, and characterized by elemental analysis, IR spectra. The X-ray crystal structure of the complex was determined. The complex crystallizes in the Monoclinic system, space group p2(1)/n with a = 10.418(4) A, b = 8.526(3) A, c = 14.319(5) A, β = 105.700(5)°, V = 1224.3(8) A3, Z = 4. The complex has two-dimensional motif. The complex and free ligand display photoluminescence at room temperature. A quasi-reversible redox couple for the complex is observed.

Efficient synthesis and in vitro antifungal activity of 1H-benzimidazol-1-yl acetates/propionates containing 1H-1,2,4-triazole moiety

A series of novel 1H-benzimidazol-1-yl acetates and 1H-benzimidazol-1-yl propionates containing 1H-1,2,4-triazole moiety were synthesized under microwave irradiation by multi-step reactions, in yields of 87-94%. Their in vitro antifungal activities against Botrytis cinerea and Sclerotinia sclerotiorum were evaluated by mycelial growth rate method. All the target compounds exhibit high activities against B. cinerea with the EC50 values of 7.96-21.74 μg/mL, higher than that of carbendazim.