338422-62-1

Basic information

• Product Name: 1-(4-FLUOROPHENYL)-2-([5-(HYDROXYMETHYL)-1-METHYL-1H-IMIDAZOL-2-YL]SULFANYL)-1-ETHANONE
• Synonyms: 4'-FLUORO-2-[5-(HYDROXYMETHYL)-1-METHYL-1H-IMIDAZOL-2-YLTHIO]ACETOPHENONE;1-(4-FLUOROPHENYL)-2-([5-(HYDROXYMETHYL)-1-METHYL-1H-IMIDAZOL-2-YL]SULFANYL)-1-ETHANONE
• CAS NO: 338422-62-1
• Molecular Formula: C13H13FN2O2S
• Molecular Weight: 280.32
• Mol File: 338422-62-1.mol

Chemical Properties

• Melting Point: 121-123°C
• Appearance: /
• CAS DataBase Reference: 1-(4-FLUOROPHENYL)-2-([5-(HYDROXYMETHYL)-1-METHYL-1H-IMIDAZOL-2-YL]SULFANYL)-1-ETHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-FLUOROPHENYL)-2-([5-(HYDROXYMETHYL)-1-METHYL-1H-IMIDAZOL-2-YL]SULFANYL)-1-ETHANONE(338422-62-1)
• EPA Substance Registry System: 1-(4-FLUOROPHENYL)-2-([5-(HYDROXYMETHYL)-1-METHYL-1H-IMIDAZOL-2-YL]SULFANYL)-1-ETHANONE(338422-62-1)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 338422-62-1(Hazardous Substances Data)

Usage

Ketone

A carbonyl group (C=O) bonded to two carbon-containing groups
The presence of a carbonyl group suggests that 1-(4-FLUOROPHENYL)-2-([5-(HYDROXYMETHYL)-1-METHYL-1H-IMIDAZOL-2-YL]SULFANYL)-1-ETHANONE may have reactivity typical of ketones, such as nucleophilic addition and enolization.

Fluorophenyl group

A phenyl ring (C6H5) with one hydrogen atom replaced by a fluorine atom
The fluorophenyl group may contribute to the compound's lipophilicity and potentially affect its biological activity.

Imidazole derivative

A compound based on the imidazole ring system (a five-membered ring with two nitrogen atoms)
Imidazole derivatives are known for their diverse biological activities, and the presence of this group in the compound suggests potential interactions with biological systems.

Hydroxymethyl group

A hydroxyl group (-OH) attached to a methyl group (-CH3)
The hydroxymethyl group may be involved in hydrogen bonding and could influence the compound's solubility and reactivity.

Sulfonyl group

A sulfur-containing group with a double bond to oxygen and a single bond to another atom or group
The presence of a sulfonyl group may affect the compound's polarity and potentially its interactions with biological targets.

Potential applications

Pharmaceutical research and drug development
Given the compound's structure and the presence of biologically relevant groups, it may have potential uses in the development of new drugs or therapeutic agents.

Further research needed

To fully understand the properties and potential uses of the compound
While the compound's structure suggests potential biological activity, more research is required to determine its specific interactions with biological systems and its suitability for pharmaceutical applications.