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

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

Uses

Used in Chemical Synthesis Industry:
2-Propyl-1H-Indene is used as a key intermediate in the synthesis of various chemical compounds for different applications. Its unique chemical structure and properties make it a valuable component in the production of other substances.
Used in Pharmaceutical Industry:
2-Propyl-1H-Indene may be utilized as a building block in the development of pharmaceutical compounds, contributing to the creation of new drugs with potential therapeutic benefits.
Used in Research and Development:
Due to its unique chemical properties, 2-Propyl-1H-Indene can be employed in research and development settings to explore its potential applications and interactions with other compounds, further expanding its use in various industries.

Upstream product

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

Downstream Products

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

Synthesis of Biological Markers in Fossil Fuels. 2. Synthesis and 13C NMR Studies of Substituted Indans and Tetralins

Unambiguous syntheses of all possible methyl, ethyl, n-propyl, and n-butyl derivatives of indan and tetralin were developed using the Kumada coupling procedure involving the reaction of aryl or vinyl halides with Grignard reagents in the presence of nickel(II) chloride.An analysis of the 13C NMR spectra of these compounds was also completed.