cis-4-Decene

Base Information

• Chemical Name: cis-4-Decene
• CAS No.: 19398-88-0
• Molecular Formula: C10H20
• Molecular Weight: 140.269
• Nikkaji Number: J97.372F
• Mol file: 19398-88-0.mol

Synonyms:cis-4-Decene;(Z)-dec-4-ene;19398-88-0;(Z)-4-Decene;4-Decene, (Z)-;(Z)-4-C10H20;(4Z)-4-Decene #;SOVOPSCRHKEUNJ-CLFYSBASSA-N

Chemical Property of cis-4-Decene

Chemical Property:

• Vapor Pressure: 2.08mmHg at 25°C
• 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: 72.1

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCC=CCCC
• Isomeric SMILES: CCCCC/C=C\CCC

Technology Process of cis-4-Decene

There total 19 articles about cis-4-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: 96.0%

4-decyne (2384-86-3) → (Z)-dec-4-ene (19398-88-0) + trans-4-Decen (19398-89-1)

Guidance literature:

With formic acid; dihydridotetrakis(triphenylphosphine)ruthenium; In N,N-dimethyl-formamide; at 20 ℃; for 36h; optical yield given as %de; stereoselective reaction; Inert atmosphere;

DOI:10.1002/chem.201001143

Reference yield: 11.0%

cis-5-decene (7433-78-5) → decane (124-18-5) + (E)-5-decene (7433-56-9) + trans-3-decene (19150-21-1) + (Z)-dec-4-ene (19398-88-0) + trans-4-Decen (19398-89-1) + 1-deuteriodecane (71941-72-5)

Guidance literature:

With Schwartz's reagent; water-d2; In toluene; at 40 ℃; for 4h; Product distribution; Mechanism; variation of time, amount of reagent, further olefins, deuterium labelling experiments;

DOI:10.1016/0022-328X(89)80053-1

Reference yield: 2.8%

1-penten (109-67-1) → 2-propylhept-1-ene (33717-91-8) + (Z)-pent-2-ene (627-20-3) + (E)-pent-2-ene (646-04-8) + trans-3-decene (19150-21-1) + (Z)-dec-4-ene (19398-88-0) + trans-4-Decen (19398-89-1) + cis-3-decene (19398-86-8)

Guidance literature:

2-[1-(2,4,6-trimethylphenylimino)ethyl]-6-[1-(4-eicosanoxy-3,5-diphenylphenylimino)ethyl]pyridine cobalt[II] chloride tetrakis[3,5-bis(trifluoromethyl)phenyl]borate; trimethylsilylmethyllithium; at 20 ℃; under 750.075 Torr; Product distribution / selectivity;

upstream raw materials:

cis-5-decene

5-Decyl-p-toluolsulfonat

Toluene-4-sulfonic acid 1-propyl-heptyl ester

cis-4-decene oxide

Downstream raw materials:

trans-4-Decen

Refernces

• 1、 Zilbershtein, Timur M.,Kardash, Vladislav A.,Suvorova, Vladlena V.,Golovko, Anatoly K.. "Decene formation in ethylene trimerization reaction catalyzed by Cr-pyrrole system". . p. 371 - 378. Retrieved 2014/03/21.
• 2、 Chung, Jooyoung,Kim, Chanhoi,Jeong, Hansaem,Yu, Taekyung,Binh, Do Huy,Jang, Jyongsik,Lee, Jaichan,Kim, B. Moon,Lim, Byungkwon. "Selective semihydrogenation of alkynes on shape-controlled palladium nanocrystals". . p. 919 - 925. Retrieved 2013/08/25.