1-Nonene

Base Information

• Chemical Name: 1-Nonene
• CAS No.: 124-11-8
• Molecular Formula: C9H18
• Molecular Weight: 126.242
• Hs Code.: 2901299090
• European Community (EC) Number: 204-681-7
• NSC Number: 73961
• UN Number: 1993
• UNII: YPK83LUD6G
• DSSTox Substance ID: DTXSID2059562
• Nikkaji Number: J43.439F
• Wikipedia: 1-Nonene
• Wikidata: Q15687205
• Metabolomics Workbench ID: 5021
• Mol file: 124-11-8.mol

Synonyms:1-n-Nonene;NSC 73961; n-Non-1-ene; a-Nonene

Chemical Property of 1-Nonene

Chemical Property:

• Appearance/Colour: Colorless liquid
• Vapor Pressure: 5.77mmHg at 25°C
• Melting Point: ?81 ºC
• Boiling Point: 146 ºC
• Flash Point: 24 ºC
• PSA: 0.00000
• Density: 0.73
• LogP: 3.53290
• XLogP3: 5.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 6
• Exact Mass: 126.140850574
• Heavy Atom Count: 9
• Complexity: 55.1
• Transport DOT Label: Flammable Liquid

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Hazard Codes: Xn:Harmful
• Statements: R10:; R36/37/38:; R65:
• Safety Statements: S26:; S36:; S62:

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 1-Nonene

There total 133 articles about 1-Nonene 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: 82.0%

dichloromethane (75-09-2) + n-octylmagnesium chloride (38841-98-4) → non-1-ene (124-11-8) + hepatdecane (629-78-7)

Guidance literature:

With C₃₁H₃₇ClN₃NiO₂^(1-)*Li⁽¹⁺⁾; In tetrahydrofuran; at 25 ℃; for 0.333333h; Overall yield = 95 %; Inert atmosphere;

DOI:10.1016/j.molcata.2012.07.007

Reference yield: 65.0%

2-nonenyl alcohol (31502-14-4) → nonane (111-84-2) + non-1-ene (124-11-8) + 2-nonene (6434-78-2) + nonyl alcohol (143-08-8)

Guidance literature:

With methanol; toluene-4-sulfonic acid; at 25 ℃; for 5h; Reagent/catalyst; Inert atmosphere; Sealed tube; UV-irradiation;

Reference yield: 17.0%

(E)-1-chloro-2-nonene (67242-74-4) → non-1-ene (124-11-8) + 2-nonene (6434-78-2)

Guidance literature:

With sodium formate; PdCl22; In n-heptane; water; for 6h; Heating;

DOI:10.1246/cl.1986.1463

upstream raw materials:

3-ethyl-dodec-5-en-3-ol

1-nonyne

dinonylsulfane

nonyl acetate

Downstream raw materials:

1,2-Nonanediol

nonyl-phosphonic acid dimethyl ester

decyl-nonyl-diphenyl-silane

methyl-nonyl-phenyl-silane

Refernces

• 1、 Miyaura,N. et al.. "-". . p. 2199 - 2200. Retrieved 1977.
• 2、 Derzhinskii, A. R.,Kalugin, V. E.,Prilezhaeva, E. N.. "ORGANIC SULFUT COMPOUNDS CONTAINING FUNCTIONAL GROUPS COMMUNICATION 5. SYNTHESIS OF α,β-EPOXYALKYL SULFONES". . p. 1225 - 1231. Retrieved 1982.
• 3、 Alexakis,A. et al.. "-". . p. 293 - 298. Retrieved 1979.
• 4、 Li, Gao,Jin, Rongchao. "Gold nanocluster-catalyzed semihydrogenation: A unique activation pathway for terminal alkynes". . p. 11347 - 11354. Retrieved 2014.
• 5、 -. "A Method for preparing alpha-olefins from Biomass-derived fat and oil". Paragraph 0191-0202; 0224-0227. . Retrieved 2020/09/22.
• 6、 -. "Method for catalytically oxidizing primary alcohol into corresponding carboxylic acid and simultaneously co-producing corresponding alpha olefin". Paragraph 0038-0039. . Retrieved 2020/12/30.