210628-07-2

Basic information

• Product Name: 4-CHLORO-2-METHYL-1H-INDENE
• Synonyms: 4-CHLORO-2-METHYL-1H-INDENE;4-Chloro-2-methylindene
• CAS NO: 210628-07-2
• Molecular Formula: C₁₀H₉Cl
• Molecular Weight: 164.63
• Mol File: 210628-07-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 249.8 °C at 760 mmHg
• Flash Point: 85.5 °C
• Appearance: /
• Density: 1.161 g/cm³
• Vapor Pressure: 0.0355mmHg at 25°C
• Refractive Index: 1.586
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-CHLORO-2-METHYL-1H-INDENE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-2-METHYL-1H-INDENE(210628-07-2)
• EPA Substance Registry System: 4-CHLORO-2-METHYL-1H-INDENE(210628-07-2)

Safety Data

• Hazardous Substances Data: 210628-07-2(Hazardous Substances Data)

Usage

General Description

4-CHLORO-2-METHYL-1H-INDENE is a chemical compound with the molecular formula C10H9Cl. It is a halogenated derivative of indene, a bicyclic aromatic hydrocarbon. 4-CHLORO-2-METHYL-1H-INDENE is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used in organic synthesis as a building block for the creation of more complex molecules. Additionally, it is known to exhibit some toxicological properties and should be handled with care in a laboratory setting.

InChI:InChI=1/C10H9Cl/c1-7-5-8-3-2-4-10(11)9(8)6-7/h2-4,6H,5H2,1H3

Upstream product

• 1026384-14-4 C₁₀H₁₁ClO 

Downstream Products

• 386267-20-5 4-(3,5-di-tert-butylphenyl)-2-methyl-1H-indene 

Relevant articles and documents

HALOGEN SUBSTITUTED METALLOCENE COMPOUNDS FOR OLEFIN POLYMERIZATION

A metallocene compound is represented by the formula (1): wherein: M is a Group 3, 4, 5 or 6 transition metal atom, or a lanthanide metal atom, or actinide metal atom, preferably a Group 4 transition metal atom selected from titanium, zirconium or hafnium; E is a substituted or unsubstituted monocyclic or polycyclic arenyl ligand pi-bonded to M; A is a substituted or unsubstituted polycyclic arenyl ligand that is pi-bonded to M and has a different ring structure than the E ligand; at least one of the A and E ligands includes at least one halogen substituent directly bonded to an sp2 carbon at a bondable ring position; Y is a bridging group containing at least one Group 13, 14, 15, or 16 element and any single position of the ring structure of A and to any single position of the ring structure of E; and y is zero or 1, indicating the absence (y = 0) or presence (y =1) of Y; and each X is a univalent anionic ligand, or two X are joined and bound to the metal atom to form a metallocycle ring, or two X are joined to form a chelating ligand, a diene ligand, or an alkylidene ligand; provided that when E is an unsubstituted cyclopentadienyl ligand, either y is one or A is not 2-bromofluorenyl or 2,7-dibromofluorenyl.