1652-97-7

Basic information

• Product Name: 2-Tetradecene
• Synonyms: 2-Tetradecen;2-Tetradecene
• CAS NO: 1652-97-7
• Molecular Formula: C14H28
• Molecular Weight: 196.376
• Mol File: 1652-97-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2-Tetradecene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Tetradecene(1652-97-7)
• EPA Substance Registry System: 2-Tetradecene(1652-97-7)

Safety Data

• Hazardous Substances Data: 1652-97-7(Hazardous Substances Data)

Upstream product

• 77953-90-3 tetradecan-1-yl phenyl telluride 
• 1120-36-1 1-tetradecene 
• 83486-08-2 C₂₀H₃₄Br₂Te 
• 64-19-7 acetic acid 
• 7434-27-7 2-methyl-tetradecanoic acid ; sodium-salt 
• 67-56-1 methanol 
• 89357-91-5 tetradecan-2-yl phenyl selenide 

Downstream Products

• 143-07-7 lauric acid 

Relevant articles and documents

Tsuji-Wacker Oxidation of Terminal Olefins using a Palladium-Carbon Nanotube Nanohybrid

Palladium nanoparticles supported on carbon nanotubes were used in the Tsuji-Wacker oxidation. The palladium-based nanohybrid was found to be very active in combination with cuprous chloride for the selective oxidation of terminal olefins into methyl ketones. The co-catalytic system operates under very mild and sustainable conditions (room temperature, atmospheric pressure, low catalyst loading), as opposed to previously reported catalysts, and can be recycled without any loss in activity. Give it a whack: Palladium nanoparticles supported on carbon nanotubes are used in combination with cuprous chloride for the selective Tsuji-Wacker oxidation of terminal olefins into methyl ketones. The co-catalytic system operates under very mild and sustainable conditions and can be recycled without any loss in activity.

INTERNAL OLEFIN SULFONATE COMPOSITION

Provided are an internal olefin sulfonate composition which is capable of sufficiently enhancing foamability, light foam quality, and instantaneous foam dissipation property, and a cleansing composition containing the internal olefin sulfonate composition. The internal olefin sulfonate composition comprises (A) an internal olefin sulfonate having 12 carbon atoms and (B) an internal olefin sulfonate having 14 carbon atoms, wherein a content mass ratio of the component (A) to the component (B), (A/B), is from 10/90 to 90/10, and a total content of the component (A) and the component (B) in the internal olefin sulfonate is from 60 to 100% by mass.

Compatibility studies of dimethyl(phenyl)silyl group as a masked hydroxyl group in compounds containing cyclopropane rings and in compounds containing the enone functionality

Compatibility of the phenyl(dimethyl)silyl group as a masked hydroxyl group in the presence of cyclopropane rings and the enone functionality was studied. The result showed that conditions for the silyl-to-hydroxyl group conversion is not compatible with cyclopropane rings. However, under a modified two-step transformation procedure, the silyl group is converted to a hydroxyl group in the presence of an enone group without disturbing the carbon-carbon double bond, to a certain extent.