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

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

Uses

Used in Pharmaceutical Industry:
4-CHLORO-2-METHYL-1H-INDENE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-CHLORO-2-METHYL-1H-INDENE is utilized as an intermediate in the production of agrochemicals. Its incorporation aids in the creation of effective compounds for crop protection and other agricultural applications.
Used in Organic Synthesis:
4-CHLORO-2-METHYL-1H-INDENE is employed as a building block in organic synthesis. It is instrumental in the construction of more complex molecules, which can be used in a wide range of applications, from materials science to specialty chemicals.
Used in Fine Chemicals Industry:
4-CHLORO-2-METHYL-1H-INDENE is also used in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors. Its role in this industry is crucial for the production of high-quality specialty chemicals.

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.