114751-76-7

Usage

Type

Organic compound

Usage

Commonly used in the pharmaceutical industry for drug synthesis

Biological activities

Antifungal, antibacterial, antitumor properties

Application

Used as a building block in medicinal chemistry for pharmaceutical development

Potential use

Investigated for use in organic semiconductor materials

Unique properties

Nitrogen-containing heterocyclic compound

Upstream product

• 26311-45-5 4-pentylbenzoic acid 
• 79-19-6 thiosemicarbazide 
• 49763-65-7 4-pentylbenzoyl chloride 
• 685541-11-1 C₁₃H₁₉N₃OS 

Downstream Products

• 114751-65-4 6-(4-Butyl-phenyl)-2-(4-pentyl-phenyl)-imidazo[2,1-b][1,3,4]thiadiazole 
• 1233091-67-2 C₁₉H₂₀FN₅O₃S 
• 1634721-15-5 2-(3-oxo-1,2-benzothiazol-2(3H)-yl)-N-(5-(4-pentylphenyl)-1,3,4-thiadiazol-2-yl)acetamide 
• 114751-68-7 2-(4-Pentyl-phenyl)-6-[4-(4-propyl-cyclohexyl)-phenyl]-imidazo[2,1-b][1,3,4]thiadiazole 

Relevant academic research and scientific papers

Synthesis of N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol- 2(3H)-yl)acetamide derivatives promoted by carbodiimide condensation

Novel N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol-2(3H)-yl) acetamide derivatives were prepared by 1-(3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride and N-hydroxybenzotrizole condensation catalysis in a convenient and fast method

Synthesis and insecticidal activities of novel 1,3,4-thiadiazole 5-fluorouracil acetamides derivatives: An RNA interference insecticide

A series of novel 1,3,4-thiadiazole 5-fluorouracil acetamides derivatives were designed and synthesized. Their structures were confirmed by infrared, 1H NMR spectroscopy, and elemental analysis. The insecticidal activities against Tetranychus cinnabarinus

LIQUID-CRYSTALLINE IMIDAZO-1,3,4-THIADIAZOLES. I. SYNTHESIS OF 2,6-DISUBSTITUTED IMIDAZO-1,3,4-THIADIAZOLES AND THEIR MESOMORPHOUS AND SPECTRAL CHARACTERISTICS

Derivatives of imidazo-1,3,4-thiadiazole possessing a wide temperature range of smectic mesophase were obtained.The introduction of the cyclohexane fragment into the imidazole part of the molecule promotes the appearance of the nematic mesophase.The structure of the new mesogens and of the intermediates in their synthesis were confirmed by the data from IR and (13)C and (1)H NMR spectroscopy.