141719-29-1

Basic information

• Product Name: 4-Chlorobutylferroene
• Synonyms: 4-Chlorobutylferroene
• CAS NO: 141719-29-1
• Molecular Formula: C14H17ClFe
• Mol File: 141719-29-1.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 130℃ at 4hPa
• Appearance: /
• Vapor Pressure: 0Pa at 20℃
• CAS DataBase Reference: 4-Chlorobutylferroene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chlorobutylferroene(141719-29-1)
• EPA Substance Registry System: 4-Chlorobutylferroene(141719-29-1)

Safety Data

• Hazardous Substances Data: 141719-29-1(Hazardous Substances Data)

Usage

General Description

4-Chlorobutylferrocene is a chemical compound consisting of a ferrocene molecule attached to a 4-chlorobutyl group. Ferrocene is an organometallic compound with a sandwich-like structure of two cyclopentadienyl anions bound to a central iron atom. The addition of a 4-chlorobutyl group to the ferrocene molecule enhances the chemical's reactivity and potential applications. 4-Chlorobutylferroene is commonly used in organic synthesis, catalysis, and as a precursor for a variety of functionalized ferrocene derivatives. Its unique structure and reactivity make it a valuable tool in the development of new chemical reactions and materials. Additionally, its potential pharmacological and biological properties make it a subject of interest for medicinal chemistry research.

Upstream product

• 5891-21-4 5-chloro-2-pentanone 
• 102-54-5 ferrocene 
• 4635-59-0 4-Chlorobutanoyl chloride 

Relevant articles and documents

Synthesis and study of electrochemical behavior of new 4-ferrocenylbutylamine derivatives

Ferrocene derivatives play important roles in the fields of biological, material and synthetic chemistries. Some 4-ferrocenylbutylamine derivatives were synthesized by the nucleophilic-substitution reactions of 4-bromobutylferrocene with various aliphatic

Derivatization of valproic acid using ferrocene derivatives: Synthesis, characterization and investigation of optical and electrochemical properties

New ferrocenyl-based valproic acid (VPA) ester derivatives were designed and synthesized according to the reaction of appropriate haloalkylferrocene derivatives with VPA in the presence of K2CO3 and a catalytic amount of 18-crown-6 ether. Elemental analyses and Fourier transform infrared, 1H NMR, 13C NMR and mass spectra all well confirmed the predicted molecular structure. This is the first report in which ferrocene has been applied in derivatization of VPA as a chromogenic group. The electrochemical properties of the synthesized compounds were studied using cyclic voltammetry measurements, and energies of the frontier molecular orbitals were determined. In addition, the solubilities of the final compounds were studied in distilled water, phosphate buffer (pH?=?7.4) and 0.9% (w/v) NaCl solution.

Highly efficient reduction of ferrocenyl aldehyde and ketones in ionic liquids

For the first time ferrocenyl aldehyde and ketones were effectively reduced to alkylferrocene using sodium borohydride and aluminum chloride in an ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIm]BF4). Mild reaction conditions,