5-Decene

Base Information

• Chemical Name: 5-Decene
• CAS No.: 19689-19-1
• Molecular Formula: C10H20
• Molecular Weight: 140.269
• European Community (EC) Number: 243-226-7
• DSSTox Substance ID: DTXSID00864063
• Wikidata: Q30118589
• Mol file: 19689-19-1.mol

Synonyms:5-Decene;Dec-5-ene;19689-19-1;EINECS 243-226-7;(5E)-5-Decene;DTXSID00864063;FT-0604946;FT-0694761;Q30118589

Chemical Property of 5-Decene

Chemical Property:

• Vapor Pressure: 2.08mmHg at 25°C
• Melting Point: -73°C
• Refractive Index: 1.4331
• Boiling Point: 169°Cat760mmHg
• Flash Point: 45.5°C
• PSA: 0.00000
• Density: 0.749g/cm³
• LogP: 3.92300
• XLogP3: 4.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 6
• Exact Mass: 140.156500638
• Heavy Atom Count: 10
• Complexity: 62.1

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Chemical Classes: Other Classes -> Aliphatics, Unsaturated
• Canonical SMILES: CCCCC=CCCCC

Technology Process of 5-Decene

There total 59 articles about 5-Decene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

1-Decene (872-05-9,17438-89-0,25189-70-2) → 5-decene (19689-19-1) + 4-decene (19689-18-0) + trans-3-decene (19150-21-1) + Decan-2-one (693-54-9) + 2-decene (20063-97-2,20348-51-0,6816-17-7)

Guidance literature:

With oxygen; 2,6-di-O-methyl-β-cyclodextrin; palladium(II) sulfate; H₉PV₆Mo₆O₄₀; copper(II) sulfate; In water; at 80 ℃; for 6h; under 750.06 Torr; Mechanism; Product distribution; influence of composition of catalytic mixture on selectivity of reaction;

Reference yield: 77.0%

1-hexene (592-41-6,25067-06-5) → ethene (74-85-1) + 5-decene (19689-19-1)

Guidance literature:

silica gel; methyltrioxorhenium(VII); In dichloromethane; for 0.5h; Heating; olefin metathesis; further alkenes;

Reference yield: 26.0%

C12H24B(1-)*Li(1+) (121826-81-1) → 2-Methyl-2-heptanol (625-25-2) + hept-2-ene (592-77-8) + 5-decene (19689-19-1) + hex-1-yne (693-02-7)

Guidance literature:

Yield given. Multistep reaction. Further byproducts given;

DOI:10.1016/S0040-4039(00)80450-5

upstream raw materials:

(E)-1,4-dibromobutene

n-propylmagnesium bromide

propyl bromide

buta-1,3-diene

Downstream raw materials:

1-hexene

diethyl 19-octadecene-1,18-dioate

myristoleic acid ethyl ester

Ethyl-tetradec-9-enoate

Refernces

Z -selective ethenolysis with a ruthenium metathesis catalyst: Experiment and theory

10.1021/ja4010267

The research involves several key chemicals that play crucial roles in the investigation of Z-selective ethenolysis and cross metathesis reactions. Methyl Oleate (6) is a standard substrate used to compare the ethenolysis reactivity and selectivity of metathesis catalysts. It is a fatty acid ester commonly used in olefin metathesis studies. 5-Decene (11) is an internal olefin used in cross metathesis reactions. The study investigates the reactivity of catalysts 3 and 5 with both cis- and trans-isomers of 5-decene. 8-Nonenyl Acetate (14) is another internal olefin substrate used in cross metathesis reactions. It is used in combination with 5-decene to study the formation of cross products.

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