79538-90-2

Basic information

• Product Name: 2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-
• Synonyms: 2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-;2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-3H-1,2,4-triazol-3- one;2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]- one;2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-3H-1,2,4-triazol-3-\none
• CAS NO: 79538-90-2
• Molecular Formula: C₁₈H₁₉N₅O₂
• Molecular Weight: 337.37576
• Product Categories: Aromatics;Bases & Related Reagents;Heterocycles;Nucleotides
• Mol File: 79538-90-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-(79538-90-2)
• EPA Substance Registry System: 2,4-Dihydro-4-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-(79538-90-2)

Safety Data

• Hazardous Substances Data: 79538-90-2(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 79538-90-2 differently. You can refer to the following data:
1. An intermediate of SCH 51048
2. An intermediate of SCH 51048, an antifungal agent.

Upstream product

• 74853-07-9 2,4-dihydro-4-[4-[4-(4-methoxyphenyl)-1-piperazinyl ]-phenyl]-3H-1,2,4-triazol-3-one 

Downstream Products

• 186806-36-0 4-[4-(4-{4-[(2R,5R)-5-(2,4-Difluoro-phenyl)-5-[1,2,4]triazol-1-ylmethyl-tetrahydro-furan-2-ylmethoxy]-phenyl}-piperazin-1-yl)-phenyl]-2-(2-methoxy-ethoxymethyl)-2,4-dihydro-[1,2,4]triazol-3-one 
• 475652-61-0 4-[4-(4-{4-[(2R,5R)-5-(2,4-Difluoro-phenyl)-5-[1,2,4]triazol-1-ylmethyl-tetrahydro-furan-2-ylmethoxy]-phenyl}-piperazin-1-yl)-phenyl]-2-hydroxymethyl-2,4-dihydro-[1,2,4]triazol-3-one 
• 475652-60-9 4-{4-[4-(4-hydroxy-phenyl)-piperazin-1-yl]-phenyl}-2-(2-methoxy-ethoxymethyl)-2,4-dihydro-[1,2,4]triazol-3-one 

Relevant articles and documents

Synthesis and antifungal activity of the 2,2,5-tetrahydrofuran regioisomers of SCH 51048

The four 2,2,5-regioisomer counterparts of SCH 51048 were synthesized and evaluated. As with the parent series, only the two cis isomers possessed any in vitro activity, and only the activity of the isomer with the R-configuration at the tetrahydrofuran 2-carbon was significant. The activity data suggests that oxygen at only one of the two possible ring positions benzylic to the difluorobenzene participates usefully in active site binding.