6301-00-4

Usage

Properties and Specific Content of 1-Hexyl-1H-Indene

The chemical formula of 1-hexyl-1H-indene consists of 16 carbon atoms and 20 hydrogen atoms.

Indene Derivative

Structure
1-hexyl-1H-indene is derived from the indene core structure, which is a bicyclic aromatic compound consisting of a six-membered benzene ring fused to a five-membered ring.

Hexyl Substituent

Alkyl Group
A hexyl substituent is a straight-chain alkyl group with six carbon atoms (C6H13) attached to the first position of the indene core.

Synthesis

Organic Compounds and Polymers
1-hexyl-1H-indene is commonly used as a starting material or intermediate in the synthesis of various organic compounds and polymers, contributing to its importance in organic chemistry.

Unique Structure

Reactivity and Versatility
The unique structure of 1-hexyl-1H-indene, with the hexyl group attached to the indene core, imparts specific reactivity and versatility to the compound, making it valuable in a wide range of applications.

Applications

Specialty Chemicals, Pharmaceuticals, and Agrochemicals
Due to its reactivity and versatility, 1-hexyl-1H-indene is used in the production of specialty chemicals, pharmaceuticals, and agrochemicals, highlighting its importance in these industries.

Potential Use

Building Block for New Materials and Chemical Processes
Researchers have studied 1-hexyl-1H-indene as a potential building block for the development of new materials and chemical processes, further expanding its potential applications and significance in the field of organic chemistry.

Upstream product

• 13249-60-0 2-bromo-1-octene 
• 40138-16-7 2-formylbenzene boronic acid 
• 111-25-1 1-bromo-hexane 
• 95-13-6 1-indene 

Relevant academic research and scientific papers

Electrochemical Synthesis of Soluble Poly(9-hexylfluorene) and Poly(1-hexylindene)

Electrochemical oxidation of 9-hexylfluorene and 1-hexylindene in 0.1 mol dm-3 Bu4NBF4-nitromethane affords ?-conjugated polymers, PHF and PHI, respectively, which are fusible and soluble in common organic solvents.Electrode materials affect the formation of the polymers significantly; the molecular weight of PHF increases in the order, glassy carbon (GC) -1, respectively, at room temperature.

Rhodium(II)- or Copper(I)-Catalyzed Formal Intramolecular Carbene Insertion into Vinylic C(sp2)?H Bonds: Access to Substituted 1H-Indenes

A rhodium(II)- or copper(I)-catalyzed formal intramolecular carbene insertion into vinylic C(sp2)?H bonds is reported herein. This method provides straightforward access to 1H-indenes with high efficiency and excellent functional-group compatibility. Mechanistically, the reaction is proposed to involve the following sequence: metal carbene formation, intramolecular nucleophilic addition of the double bond to the electron-deficient carbene carbon atom, dearomatization, and finally a 1,5-H shift.

Amido functionalized ansa half-sandwich dichloride complexes of titanium, zirconium and hafnium with alkyl and ω-alkenyl substituents as homogeneous and self-immobilizing catalyst precursors for ethylene polymerization

A total of 24 amido functionalized ansa half-sandwich dichloride complexes of titanium, zirconium and hafnium with cyclopentadienyl or indenyl ligands have been prepared, characterized and used for catalytic ethylene polymerization. Alkyl and ω-alkenyl substituents on the aromatic system influence the polymerization activity of the catalysts and the properties of the produced polyethylene. After activation with methylalumoxane the ω-alkenyl substituted catalysts show self-immobilization in ethylene polymerization.