39187-97-8

Basic information

• Product Name: 2-(4-fluorophenyl)thiazole
• Synonyms: 2-(4-fluorophenyl)thiazole
• CAS NO: 39187-97-8
• Molecular Formula: C₁₀H₉NS
• Molecular Weight: 175.2502
• Mol File: 39187-97-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 296.9 °C at 760 mmHg
• Flash Point: 137.2 °C
• Appearance: /
• Density: 1.14 g/cm³
• Vapor Pressure: 0.00246mmHg at 25°C
• Refractive Index: 1.593
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(4-fluorophenyl)thiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-fluorophenyl)thiazole(39187-97-8)
• EPA Substance Registry System: 2-(4-fluorophenyl)thiazole(39187-97-8)

Safety Data

• Hazardous Substances Data: 39187-97-8(Hazardous Substances Data)

Usage

General Description

2-(4-fluorophenyl)thiazole is a chemical compound with the molecular formula C9H6FNS. It is a thiazole derivative with a fluorophenyl group attached to the 2-position of the thiazole ring. 2-(4-fluorophenyl)thiazole has potential applications in the field of pharmaceuticals, agrochemicals, and material science. It may be used as a building block in the synthesis of various biologically active molecules and agrochemicals. Additionally, its unique chemical structure makes it a valuable component in the development of new materials with specific properties. The compound's potential uses in various industries make it an interesting target for further research and development.

InChI:InChI=1/C10H9NS/c1-8-4-2-3-5-9(8)10-11-6-7-12-10/h2-7H,1H3

Upstream product

• 3034-53-5 2-bromo-1,3-thiazole 
• 16419-60-6 2-Methylphenylboronic acid 
• 1826-11-5 2-phenylthiazole 
• 823-96-1 Trimethylboroxine 
• 288-47-1 1,3-thiazole 
• 615-37-2 ortho-methylphenyl iodide 

Downstream Products

• 1078735-71-3 C₁₇H₁₅NOS 
• 1078735-75-7 C₂₀H₁₅NS 
• 1021602-72-1 C₂₀H₁₆N₂S₂ 
• 1217887-61-0 C₁₁H₈F₃NS 
• 1236376-58-1 2-(2,6-dimethylphenyl)thiazole 

Relevant articles and documents

Aromatic C-H Methylation and Other Functionalizations via the Rh(III)-Catalyzed Migratory Insertion of Bis(phenylsulfonyl)carbene and Subsequent Transformations

The Rh(III)-catalyzed migratory insertion of bis(phenylsulfonyl)carbene into aromatic C-H bonds has been developed. A variety of bis(phenylsulfonyl)methyl derivatives were prepared with good yields under mild conditions. The methylated products were readily obtained after reductive desulfonylation. Furthermore, the diverse transformations of bis(phenylsulfonyl)methyl to trideuteriomethyl, aldehyde, and other functional groups were demonstrated.

Rhodium(III)-Catalyzed ortho -C-H Alkylation of 2-Arylbenzothiazoles and 2-Arylthiazoles with Potassium Alkyltrifluoroborates

A general and efficient Rh(III)-catalyzed ortho-C-H alkylation of 2-arylbenzothizazoles and 2-arylthiazoles with potassium alkyltrifluoroborates has been developed. The present method leads to the construction of a library of alkylated 2-arylbenzothiazole

Efficient coupling of heteroaryl halides with arylboronic acids in the presence of a palladium-tetraphosphine catalyst

Cis, cis, cis-1,2,3,4-tetrakis(diphenylphosphinomethyl) cyclopentane: ·1/2[PdCl(C3H5)]2 system catalyses the Suzuki cross-coupling of heteroaryl halides with a range of arylboronic acids with very high ratio substrate/catalyst in good yields. Substrates such as pyridines, quinolines, thiophenes, an indole, pyrimidines or a furane have been used successfully.