92013-11-1

Basic information

• Product Name: 2-PROPYL-1 H-INDENE
• Synonyms: 2-PROPYL-1 H-INDENE
• CAS NO: 92013-11-1
• Molecular Formula: C₁₂H₁₄
• Molecular Weight: 158.24
• Product Categories: Indanone & Indene
• Mol File: 92013-11-1.mol
• Article Data: 2

Chemical Properties

• Melting Point: 71.5°C (estimate)
• Boiling Point: 78°C 0.5 mm Hg
• Flash Point: 219°C
• Appearance: /
• Density: 0.95 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.551(lit.)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-PROPYL-1 H-INDENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PROPYL-1 H-INDENE(92013-11-1)
• EPA Substance Registry System: 2-PROPYL-1 H-INDENE(92013-11-1)

Safety Data

• Hazardous Substances Data: 92013-11-1(Hazardous Substances Data)

Usage

General Description

2-Propyl-1 H-Indene is a chemical compound that primarily used in the manufacture of other substances. It is a moderately toxic substance that can cause skin, eye, and respiratory irritation if direct exposure occurs. Short, repeated exposure to high concentrations of 2-Propyl-1 H-Indene can result in unconsciousness and in extreme cases, could be fatal. Prolonged exposure may also be harmful to kidneys and liver. It's important to handle this substance under strict safety measures to prevent accidental ingestion or inhalation. Sustainable disposal methods should be used to prevent environmental contamination since they may pose toxic effects on aquatic organisms. In chemical properties, this compound belongs to the class of organic compounds known as indenes and isoindenes. It exhibits properties like being insoluble in water and having a high boiling point. It's produced synthetically and not naturally occurring.

Upstream product

• 10485-09-3 2-bromoindene 
• 92013-10-0 2-propylindan-1-one 
• 83-33-0 inden-1-one 
• 2234-82-4 1-propylmagnesium chloride 

Downstream Products

• 361211-95-2 C₉H₆(CH₂)C₆H₅ZrCl₂C₉H₆(CH₂)2CH₃ 
• 361212-03-5 C₉H₆(CH₂)2C₆H₅ZrCl₂C₉H₆(CH₂)2CH₃ 

Relevant articles and documents

Substituted indenyl containing metal complexes and olefin polymerization process

PCT No. PCT/US96/16012 Sec. 371 Date Feb. 19, 1998 Sec. 102(e) Date Feb. 19, 1998 PCT Filed Oct. 3, 1996 PCT Pub. No. WO97/15583 PCT Pub. Date May 1, 1997Group 4 metal complexes comprising an indenyl group substituted in the 2 or 3 position with at least one group selected from hydrocarbyl, fluoro-substituted hydrocarbyl, hydrocarbyloxy-substituted hydrocarbyl, dialkylamino-substituted hydroacrbyl, silyl, germyl and mixtures thereof, said indenyl group further being covalently bonded to the metal by means of a divalent ligand group, catalytic derivatives thereof and their use as olefin polymerization catalysts are disclosed.