4848-71-9

Basic information

• Product Name: 1-(3-chloro-4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazo[4,5-b]quinoxaline
• Synonyms: 1H-Imidazo[4,5-b]quinoxaline, 1-(3-chloro-4-fluorophenyl)-2-(4-nitrophenyl)-
• CAS NO: 4848-71-9
• Molecular Formula: C₉H₁₄SeSn
• Molecular Weight: 419.7957
• Mol File: 4848-71-9.mol

Chemical Properties

• Boiling Point: 662.3°C at 760 mmHg
• Flash Point: 354.3°C
• Density: 1.55g/cm³
• Vapor Pressure: 2.07E-17mmHg at 25°C
• Refractive Index: 1.747
• CAS DataBase Reference: 1-(3-chloro-4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazo[4,5-b]quinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-chloro-4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazo[4,5-b]quinoxaline(4848-71-9)
• EPA Substance Registry System: 1-(3-chloro-4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazo[4,5-b]quinoxaline(4848-71-9)

Safety Data

• Hazardous Substances Data: 4848-71-9(Hazardous Substances Data)

Usage

Fused tricyclic structure

The compound has a complex structure with three fused rings, which contributes to its unique properties and potential applications.

Chloro and fluorophenyl group

The presence of a chloro and fluorophenyl group in the molecule can influence its reactivity, stability, and interaction with biological targets.

Nitrophenyl group

The nitrophenyl group is an important functional group that can affect the compound's reactivity, stability, and potential biological activity.

Imidazoquinoxaline core

The core structure of the compound is an imidazoquinoxaline, which is a heterocyclic compound with potential biological and pharmacological activities.

Potential biological and pharmacological activities

Due to its unique structure, the compound may interact with specific biological targets, making it a candidate for further research in the development of pharmaceutical drugs or as a chemical tool in biological research.

Further studies needed

To fully understand the properties and potential uses of this compound, additional research is required, including studies on its reactivity, stability, and interactions with biological targets.

Applications in drug development

If the compound demonstrates promising biological activity, it may be used in the development of new pharmaceutical drugs targeting specific diseases or conditions.

Chemical tool in biological research

The compound's unique structure and potential biological activity make it a valuable tool for researchers studying various biological processes and mechanisms.

Reactivity and stability

The compound's reactivity and stability are influenced by its functional groups and core structure, which can be important factors in its potential applications and further research.

Interactions with biological targets

The compound's potential to interact with specific biological targets is a key factor in its potential use in drug development and biological research.

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Relevant articles and documents

Novel room light-induced disproportionation reaction of organo-ditin and -dilead compounds with organic dichalcogenides: An efficient salt-free route to organo-tin and -lead chalcogenides

Disproportionation of organo-ditin and -dilead compounds (R3M)2 (M = Sn, Pb) with organic dichalcogenides (R'Z)2 (Z = S, Se, Te) is efficiently promoted by room light to produce the corresponding organo-tin and -lead chalc

Reactions of RSe-EMe3 (E = Si, Ge, Sn, Pb) with XeF2 - RSe-F equivalents in the fluoroselenenylation of acetylenes

Selenides of the type R1Se-EMe3 (E = Si, Ge, Sn, Pb) react with xenon difluoride by cleavage of the Se-E bond to yield the R1Se-F intermediate and the fluorides Me3E-F, whereas the Se-C bond in PhSe-tBu (E = C) is stable against XeF2. The presence of R1Se-F intermediates is confirmed by addition to acetylenes (4-octyne, 3-hexyne). Thus, the fluoroselenenylation of acetylenes gives fluoro(organylseleno)olefins in preparative yields. In the cases of E = Si, Ge, Sn, and Pb, aryl and n-alkyl groups are suitable as the substituent R1. The X-ray crystal structural analysis of (E)-3-(p- carboxyphenylseleno)-4-fluorohex-3-ene - the first example of an uncharged fluoroselenoolefin synthesized from p-EtO2C-C6H4-Se-SnMe3, XeF2, and 3- hexyne followed by an ester hydrolysis - shows that the addition of the selenenylfluoride intermediate to the acetylene proceeds via a trans- addition, as is known for the R2Se2-XeF2 reagents.