19398-37-9

Basic information

• Product Name: 3-Decene
• Synonyms: 3-Decene
• CAS NO: 19398-37-9
• Molecular Formula: C₁₀H₂₀
• Molecular Weight: 140.27
• Mol File: 19398-37-9.mol
• Article Data: 7

Chemical Properties

• Melting Point: -56.93°C (estimate)
• Boiling Point: 166.82°C (estimate)
• Appearance: /
• Density: 0.7619
• Refractive Index: 1.4315
• CAS DataBase Reference: 3-Decene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Decene(19398-37-9)
• EPA Substance Registry System: 3-Decene(19398-37-9)

Safety Data

• Hazardous Substances Data: 19398-37-9(Hazardous Substances Data)

Usage

InChI:InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h5,7H,3-4,6,8-10H2,1-2H3

Upstream product

• 111-66-0 oct-1-ene 
• 872-05-9 1-Decene 
• 71-43-2 benzene 
• 334-48-5 1-decanoic acid 
• 1120-06-5 decan-2-ol 

Downstream Products

• 502-56-7 nonanone-5 

Relevant articles and documents

Liquid phase alkylation of benzene with dec-1-ene catalyzed on supported 12-tungstophosphoric acid

The liquid phase alkylation of benzene with dec-1-ene was catalyzed by 12-tungstophosphoric acid (WP) supported on different solids (ZrO2, SiO2, activated carbon and boehmite-Al2O3). Catalysts prepared with 20 w

Photocatalytic-controlled olefin isomerization over WO3–x using low-energy photons up to 625 nm

WO3–x (W-1) was used to achieve controllable photoisomerization of linear olefins without substituents under 625 nm light irradiation. Thermodynamic and kinetic isomers were obtained by regulating the carbon chain length of the olefins. Terminal olefins were converted into isomerized products, and the internal olefin mixtures present in petroleum derivatives were transformed into valuable pure olefin products. Oxygen vacancies (OVs) in W-1 altered the electronic structure of W-1 to improve its light-harvesting ability, which accounted for the high activity of olefin isomerization under light irradiation up to 625 nm. Additionally, OVs on the W-1 surface generated unsaturated W5+ sites that coordinated with olefins for the efficient adsorption and activation of olefins. Mechanistic studies reveal that the in situ formation of surface π-complexes and π-allylic W intermediates originating from the coordination of coordinated unsaturated W5+ sites and olefins ensure high photocatalytic activity and selectivity of W-1 for the photocatalytic isomerization of olefins via a radical mechanism.

Effect of the presence of ionic liquid during the NiMoS bulk preparation in the transformation of decanoic acid

The impact of the presence and amount of [BMIM][NTf2] ionic liquid during the preparation of bulk NiMoS catalysts was investigated. It was clearly shown that these factors have a strong influence on both the morphology and specific surface area of the obtained NiMoS samples. Most interestingly the catalytic activity for the transformation of decanoic acid increased up to three times when IL was present during synthesis. In the same time, a greater selectivity towards hydrocarbons was observed. On the whole a clear relationship between catalytic activity, selectivity and NiMoS morphology was demonstrated. Consequently, it is possible to modify the morphology of the materials and impact the catalytic properties by changing the synthesis conditions.