58905-26-3

Basic information

• Product Name: Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)-
• Synonyms: 1-phenyl-2-(1H-1,2,4-triazol-1-yl)Ethanone;Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)-;1-Phenyl-2-[1,2,4]triazol-1-yl-ethanone
• CAS NO: 58905-26-3
• Molecular Formula: C₁₀H₉N₃O
• Molecular Weight: 187.19796
• Mol File: 58905-26-3.mol
• Article Data: 32

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)-(58905-26-3)
• EPA Substance Registry System: Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)-(58905-26-3)

Safety Data

• Hazardous Substances Data: 58905-26-3(Hazardous Substances Data)

Usage

General Description

"Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)-" is a chemical compound with the molecular formula C10H8N4O. It is a member of the ketone and triazole families, containing a phenyl group bonded to a 1,2,4-triazole ring. Ethanone, 1-phenyl-2-(1H-1,2,4-triazol-1-yl)- has various uses and applications, including in pharmaceuticals, agriculture, and research. It can act as a building block in the synthesis of pharmaceutical compounds and can also be used as a research tool in biochemical studies. Additionally, it may have potential biological activities and could be utilized as an antifungal, antiviral, or antiparasitic agent in the field of medicine.

Upstream product

• 288-88-0 1,2,4-Triazole 
• 70-11-1 α-bromoacetophenone 
• 120669-94-5 4-Phenacyl-1,2,4-triazole 
• 118227-29-5 4-Amino-1-(2-oxo-2-phenyl-ethyl)-4H-[1,2,4]triazol-1-ium; chloride 
• 532-27-4 1-chloroacetophenone 
• 1092852-28-2 1-phenyl-2-(1,2,4-1H-triazol-1-yl)ethanone hydrochloride 
• 98-86-2 acetophenone 
• 71-43-2 benzene 

Downstream Products

• 99736-87-5 3-(4-chlorophenyl)-1-phenyl-2-(1H-1,2,4-triazol-1-yl)-propen-1-one 
• 168009-80-1 1-(2-phenyl-oxiranylmethyl)-1H-[1,2,4]triazole 
• 877875-94-0 N-[4-phenyl-5-(1,2,4-triazol-1-yl)thiazol-2-yl]amide 
• 136188-28-8 3,3,4-Trimethyl-2-phenyl-2-(1H-1,2,4-triazol-1-yl)methyloxetane 
• 1278594-45-8 2-(3,5-diphenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenyl-5-(1H-1,2,4-triazol-1-yl)-thiazole 
• 1278594-48-1 C₂₆H₁₉ClN₆S 
• 1278594-51-6 C₂₇H₂₂N₆OS 
• 1278594-54-9 C₂₆H₁₉ClN₆S 
• 1278594-57-2 C₂₆H₁₈Cl₂N₆S 
• 1278594-60-7 C₂₇H₂₁ClN₆OS 
• 99736-86-4 1-phenyl-2-(1H-1,2,4-triazolo-yl)-3-phenyl-prop-en-1-one 
• 1228047-12-8 3-(4-methoxyphenyl)-1-phenyl-2-(1H-1,2,4-triazol-1-yl)propen-1-one 

Relevant articles and documents

Asymmetric transfer hydrogenation of heterocycle-containing acetophenone derivatives using N-functionalised [(benzene)Ru(II)(TsDPEN)] complexes

The application of enantiomerically-pure ruthenium(II) catalysts containing N - functionalised TsDPEN ligand to the asymmetric transfer hydrogenation of 15 examples of α-heterocyclic acetophenone derivatives is reported. Products of up to 99% ee were formed.

Novel triazole-containing allyl benzoic acid ester compound as well as preparation method and application thereof

The invention discloses a novel triazole-containing allyl benzoic acid ester compound as well as a preparation method and application thereof. The structural formula of the novel triazole-containing allyl benzoic acid ester compound is shown as a formula

Synthesis and Biological Evaluation of Novel Triazole Derivatives as Strigolactone Biosynthesis Inhibitors

Strigolactones (SLs) are one of the plant hormones that control several important agronomic traits, such as shoot branching, leaf senescence, and stress tolerance. Manipulation of the SL biosynthesis can increase the crop yield. We previously reported tha