79442-06-1

Usage

Uses

Used in Pharmaceutical Industry:
2-(3-chlorophenyl)-5-phenyl-1,3,4-oxadiazole is used as a building block in the synthesis of various pharmaceutical drugs due to its unique chemical structure and reactivity. Its presence in drug molecules can contribute to their therapeutic effects and properties.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 2-(3-chlorophenyl)-5-phenyl-1,3,4-oxadiazole is studied for its potential antimicrobial properties. Its incorporation into antimicrobial agents can enhance their effectiveness against various microorganisms, contributing to the development of new treatments for infectious diseases.
Used in Anti-inflammatory Applications:
2-(3-chlorophenyl)-5-phenyl-1,3,4-oxadiazole is also being investigated for its anti-inflammatory potential. Its presence in anti-inflammatory drugs can help modulate the body's inflammatory response, providing relief from inflammation-related conditions and diseases.
Used in Anticancer Applications:
2-(3-chlorophenyl)-5-phenyl-1,3,4-oxadiazole has shown promise in anticancer research, where it is being studied for its potential to inhibit the growth and progression of cancer cells. Its incorporation into anticancer drugs can contribute to the development of novel therapeutic agents that target various types of cancer.

Upstream product

• 82973-10-2 3-chloro-benzoic acid benzylidenehydrazide 
• 613-94-5 benzoic acid hydrazide 
• 76591-84-9 4-(m-chloro-α-methylthiobenzylidene)morpholinium iodide 
• 41421-28-7 5-(3-chloro-phenyl)-1⁽²⁾H-tetrazole 
• 532-55-8 Benzoyl isothiocyanate 
• 587-04-2 m-Chlorobenzaldehyde 
• 611-74-5 N,N-dimethylbenzamide 
• 119072-55-8 tert-butylisonitrile 
• 625-99-0 3-iodochlorobenzene 
• 39575-05-8 N’-(3-chlorophenylmethylene)benzohydrazide 
• 65-85-0 benzoic acid 
• 825-56-9 2-phenyl-1,3,4-oxadiazole 
• 76226-60-3 (3-chlorophenyl)-morpholino-methanethione 
• 41421-28-7 5-(m-chlorophenyl)tetrazole 

Relevant academic research and scientific papers

The preparation, characterization and catalytic activity of Ni NPs supported on porous alginate-g-poly(p-styrene sulfonamide-co-acrylamide)

Herein, we report the synthesis of nickel nanoparticles under mild conditions using porous alginate-g-poly(p-styrene sulfonamide-co-acrylamide) as a protecting/stabilizing agent and sodium borohydride as a reducing agent. The porous cross-linked polymeric support was preparedviacombining the use of sol-gel, nanocasting, and crosslinking techniques, in which thep-styrene sulfonamide monomer (PSSA) andN,N′-methylene-bis (acrylamide) (MBA) cross-linker underwent copolymerization on the surface of sodium alginate in the presence of a SiO2nanoparticle (NP) template (Alg-PSSA-co-ACA). The prepared catalyst (Alg-PSSA-co-ACA@Ni) showed high catalytic activity for the one-step synthesis of 1,3,4-oxadiazoles from the reaction of hydrazides and aryl iodides through isocyanide insertion/cyclization.

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present specification provides a compound represented by chemical formula 1 and an organic light emitting device including the same. The compound may improve lifespan characteristics of the organic light emitting device.

Ligand-free Cu(ii)-mediated aerobic oxidations of aldehyde hydrazones leading to N,N′-diacylhydrazines and 1,3,4-oxadiazoles

A Cu(ii)-mediated synthesis of N,N′-diacylhydrazines and 1,3,4-oxadiazoles from aldehyde hydrazones has been developed. This is the first time that the synthesis of N,N′-diacylhydrazines and 1,3,4-oxadiazoles using N,N-dimethylamides as the acylation reagent and O2 in air as the oxidation reagent is reported. These reactions offered several advantages including simple workups, ligand-free inexpensive metal salts as mediators, high yields, and wide scope of substrates.

2,5-Diaryloxadiazoles and their precursors as novel inhibitors of cathepsins B, H and L

High levels of cathepsins indicated in various pathological conditions like arthritis, cancer progressions, and atherosclerosis explains the need to explore potential inhibitors of these proteases which can be of great therapeutic significance. We, in the present work, report the synthesis of some 2,5-diaryloxadiazoles from N-subsitutedbenzylidenebenzohydrazides. The synthesized compounds were screened for their inhibitory potential on cathepsins B, H and L. Structure Activity Relationship studies show that 2,5-diaryloxadiazoles were less inhibitory than their precursors. 1i and 2k have been found to be most inhibitory to cathepsins B and L. Their Ki values have been calculated as 11.38 × 10-8 M and 66.4 × 10-8 M for cathepsin B and 4.2 × 10-9 M and 47.31 × 10-9 M for cathepsin L, respectively. However, cathepsin H activity was maximally inhibited by compounds, 1e and 2c with Ki values of 4.4 × 10-7 M and 5.6 × 10-7 M, respectively. Enzyme kinetic studies suggest that these compounds are competitive inhibitors to the enzymes. The results have been compared with docking results obtained using iGemDock.

Photoinduced Copper-Catalyzed C-H Arylation at Room Temperature

Room-temperature azole C-H arylations were accomplished with inexpensive copper(I) compounds by means of photoinduced catalysis. The expedient copper catalysis set the stage for site-selective C-H arylations of non-aromatic oxazolines under mild reaction conditions, and provides step-economical access to the alkaloid natural products balsoxin and texamine. Copper light: Room-temperature C-H arylations of heteroarenes were accomplished with inexpensive copper compounds by photoinduced catalysis. The expedient copper catalysis leads to site-selective C-H arylations of non-aromatic oxazolines under mild reaction conditions, and provides step-economical access to the alkaloid natural products balsoxin and texamine.

Microwave-assisted one-step synthesis of 2,5-disubstituted-1,3,4- oxadiazoles using 1,4- bis(triphenylphosphonium)-2-butene peroxodisulfate

A series of 1,3,4-oxadiazoles were efficiently synthesized from the cyclization-oxidation reaction of acyl hydrazones by using 1,4- bis(triphenylphosphonium)-2-butene peroxodisulfate as an oxidant in solvent-free medium under microwave irradiation.

A novel, one-pot synthesis of 2,5-disubstituted-1,3,4-oxadiazoles using 1,4-bis(Triphenylphosphonium)-2-butene peroxodisulfate

An efficient and convenient synthesis of 1,3,4-oxadiazoles from aromatic aldehydes, acyl hydrazide, and 1,4- bis(triphenylphosphonium)-2-butene peroxodisulfate is reported. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.

Microwave assisted syntheses of 2,5-disubstituted 1,3,4-oxadiazoles

2,5-Di-substituted 1,3,4-oxadiazoles have been synthesized from the oxidation of 1-aroyl-2-arylidene hydrazines with potassium permanganate on the surface of solid mineral support as well as in the mixture of acetone and water under microwave irradiation. 2,5-Disubstituted 1,3,4-oxadiazoles have been synthesized by oxidation of 1-aroyl-2-arylidene hydrazines with potassium permanganate on the surface of a solid mineral support as well as in mixtures of acetone and water under microwave irradiation.

TETRAZOLES IN THE SYNTHESES OF 1,3,4-OXADIAZOLES

Various variants of cleavage of tetrazoles to form 1,3,4-oxadiazoles are examined.The mechanisms and synthetic potentialities of these reactions are discussed.

TETRAZOLES. XXX. ACYLATION OF 5-SUBSTITUTED TETRAZOLES

The acylation of 5-substituted tetrazoles with carboxylic acid chlorides and anhydrides gives rise to 2,5-disubstituted 1,3,4-oxadiazoles in high yields.The reaction goes without the addition of organic bases at 100-105 deg C.The acylation of 5-substituted tetrazoles in a two-phase organic solvent-water system in presence of tetrabutylammonium bromide yields N-acyltetrazoles, which are converted into 2,5-disubstituted 1,3,4-oxadiazoles on thermolysis.