110319-94-3

Basic information

• Product Name: 1H-Pyrrole,2-(4-fluorophenyl)-(9CI)
• Synonyms: 1H-Pyrrole,2-(4-fluorophenyl)-(9CI)
• CAS NO: 110319-94-3
• Molecular Formula: C₁₀H₈FN
• Molecular Weight: 161.1756232
• Product Categories: HALIDE
• Mol File: 110319-94-3.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrole,2-(4-fluorophenyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole,2-(4-fluorophenyl)-(9CI)(110319-94-3)
• EPA Substance Registry System: 1H-Pyrrole,2-(4-fluorophenyl)-(9CI)(110319-94-3)

Safety Data

• Hazardous Substances Data: 110319-94-3(Hazardous Substances Data)

Usage

Derivative of pyrrole

Heterocyclic aromatic organic compound The compound is derived from pyrrole, which is a five-membered ring structure containing four carbon atoms and one nitrogen atom, giving it unique chemical and pharmacological properties.

4-fluorophenyl group

Modification of the pyrrole ring The addition of a 4-fluorophenyl group to the pyrrole ring contributes to the compound's unique properties and potential applications in medicinal chemistry.

Potential applications

Medicinal chemistry and pharmaceutical drug development 1H-Pyrrole,2-(4-fluorophenyl)-(9CI) has potential uses in the field of medicinal chemistry, particularly in the development of new pharmaceutical drugs.

Further study and exploration

Specific properties and potential uses The compound's unique properties and potential applications require additional research and investigation to fully understand and harness its potential in the field of medicinal chemistry.

Upstream product

• 329-79-3 1-(4-fluorophenyl)ethanone oxime 
• 74-86-2 acetylene 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 22217-86-3 2-(4-fluorophenyl)-Δ¹-pyrrolidine 
• 904672-47-5 1-(4-fluorophenyl)but-3-en-1-one oxime 
• 1616603-22-5 C₁₂H₁₂FNO₂ 
• 61668-02-8 1-(4-fluorophenyl)but-3-en-1-one 
• 86718-78-7 1-(4-fluorophenyl)-3-buten-1-ol 
• 459-57-4 4-fluorobenzaldehyde 
• 109-97-7 pyrrole 
• 1868-08-2 bis(4-fluorophenyl)iodonium bromide 
• 1765-93-1 4-fluoroboronic acid 
• 116332-52-6 4-dimethylhydrazono-4-(4-fluorophenyl)butanaldimethylacetal 
• 116332-55-9 3-(1,3-dioxolan-2-yl)-1-(4-fluorophenyl)propan-1-one 

Downstream Products

• 1392440-47-9 1-[5-(4-fluorophenyl)-1H-pyrrol-2-yl]ethan-1-one 
• 1604834-02-7 C₂₂H₁₉FN₂O 

Relevant articles and documents

3,5-diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes: Synthesis, spectroscopic, electrochemical, and structural properties

This research was undertaken to obtain new 'BODIPY' dyes that fluoresce at relatively long wavelengths. The title compounds 1a-e were prepared via a divergent route involving Suzuki couplings of arylboronic acids to N-tert- butoxycarbonyl-4-bromopyrrole 2, condensation of the products with an acid chloride, and incorporation of the boron difluoride entity. Two alkyl- substituted systems 7a and 7b were also prepared for comparison; the critical difference between structures 1 and 7 is that the former have an aryl group attached to each pyrrole nucleus whereas the latter only have alkyl substituents on that same ring. UV absorption and fluorescence emission data were compared for compounds 1 and 7. Absorption and fluorescence emission maxima for compounds 1 occur at higher wavelengths than for compounds 7, and the Stokes shifts for the aryl-substituted compounds 1 are larger than for the alkyl-substituted compounds 7. Fluorescence quantum yields measured for compounds 1 are less than for compounds 7, and possible reasons for this are outlined. Other physical data for the compounds were also collected. Oxidation and reduction potentials of the systems were obtained from cyclic voltammetry experiments, and a single-crystal X-ray structure determination was performed for the bisnaphthyl-substituted compound 1b.

Synthesis of 2-arylpyrroles via catalytic dehydrogenation of 2-aryl-1-pyrrolines in the presence of palladium-supported on alumina

A convenient synthesis of 2-arylpyrroles from the catalytic dehydrogenation of 2-aryl-1-pyrrolines in the presence of commercial palladium-supported on alumina (Pd/Al2O3) is described. The reaction scope was tested for aryl substituents with different steric hindrances and electronic natures. The dehydrogenation reaction conditions such as temperature, reflux time and amount of catalyst, revealed to be highly dependent on the 2-aryl substituent group, moderate to high yields and selectivities being obtained in a reaction involving straightforward work-up and purification procedures. In addition, the synthesis of the corresponding 2-aryl-1-pyrroline starting materials, through the cyclisation reaction involving 4-chlorobutyronitrile and aryl Grignard reagents, is also reported.

Copper-catalyzed 5-endo-trig cyclization of ketoxime carboxylates: A facile synthesis of 2-arylpyrroles

A novel and facile copper-catalyzed 5-endo-trig cyclization of ketoxime carboxylates for the synthesis of 2-arylpyrroles has been developed. The reaction tolerates a range of functional groups and is a practical procedure for rapid synthesis of 2-arylpyrroles in high yields under mild conditions. the Partner Organisations 2014.

Iron-mediated direct suzuki-miyaura reaction: A new method for the ortho -arylation of pyrrole and pyridine

(Figure presented) The first example of an iron-mediated direct Suzuki-Miyaura reaction between N-heterocyclic compounds and arylboronic acids is described, and both electron-rich and electron-deficient heteroarenes can be successfully used for the coupling reaction.