4-Methyl-2-heptene

Base Information

• Chemical Name: 4-Methyl-2-heptene
• CAS No.: 3404-56-6
• Molecular Formula: C8H16
• Molecular Weight: 112.215
• DSSTox Substance ID: DTXSID101015849
• Nikkaji Number: J797.739E
• Wikidata: Q27160855
• Mol file: 3404-56-6.mol

Synonyms:4-Methyl-2-heptene;trans-4-Methyl-2-heptene;2-Heptene, 4-methyl-, (E)-;(E)-4-Methyl-2-heptene;3404-56-6;2-Heptene, 4-methyl-;66225-17-0;(2E)-4-Methyl-2-heptene;(E)-4-methylhept-2-ene;(E)-2-Heptene, 4-methyl;4-Methyl-2-heptene (trans);CHEBI:88854;SVGLFIBXFVQUQY-GQCTYLIASA-N;SVGLFIBXFVQUQY-UHFFFAOYSA-N;DTXSID101015849;Q27160855

Chemical Property of 4-Methyl-2-heptene

Chemical Property:

• Vapor Pressure: 22.8mmHg at 25°C
• Boiling Point: 115.2°Cat760mmHg
• Flash Point: 11.9°C
• PSA: 0.00000
• Density: 0.725g/cm³
• LogP: 2.99870
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 112.125200510
• Heavy Atom Count: 8
• Complexity: 62.4

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC(C)C=CC
• Isomeric SMILES: CCCC(C)/C=C/C

Technology Process of 4-Methyl-2-heptene

There total 2 articles about 4-Methyl-2-heptene 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:

(+)-R-methylisoborneol (68330-43-8,812697-60-2) → 3-ethyl-2,5-dimethylfuran (10599-62-9) + campholenyc aldehyde (4501-58-0,23727-15-3,91200-86-1,91819-58-8) + (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one (464-49-3,68546-28-1) + 2,6-dimethyl-2,4-heptadiene (4634-87-1) + 2,3,4,5-tetramethyl-2-cyclopenten-1-one (54458-61-6) + (R)-camphorquinone (10334-26-6) + 4-methylhept-2-ene (3404-56-6) + 4-methyl-3-pent-2-enyl-dihydrofuran-2-one + 1,7,7-trimethylbicyclo<2.2.1>heptan-2,5-dione (13898-78-7) + 1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-dione

Guidance literature:

With oxygen; titanium(IV) oxide; In water; at 20 ℃; for 1.66667h; Kinetics; UV-irradiation;

DOI:10.1016/j.jphotochem.2014.04.013

Reference yield:

(+)-R-methylisoborneol (68330-43-8,812697-60-2) → 3-ethyl-2,5-dimethylfuran (10599-62-9) + campholenyc aldehyde (4501-58-0,23727-15-3,91200-86-1,91819-58-8) + (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one (464-49-3,68546-28-1) + 2,6-dimethyl-2,4-heptadiene (4634-87-1) + 2,3,4,5-tetramethyl-2-cyclopenten-1-one (54458-61-6) + (R)-camphorquinone (10334-26-6) + 3,3,4-trimethylcyclohex-1-enecarbaldehyde (91055-80-0) + 4-methylhept-2-ene (3404-56-6) + 1,6,7,7-tetramethylbicyclo[2.2.1]hept-5-en-2-ol + 4-methyl-3-pent-2-enyl-dihydrofuran-2-one + 1,7,7-trimethylbicyclo<2.2.1>heptan-2,5-dione (13898-78-7) + 1,7,7-trimethylbicyclo[2.2.1]heptane-2,6-dione

Guidance literature:

With silicadodecatungstate; oxygen; In water; at 20 ℃; for 1.66667h; Kinetics; UV-irradiation;

DOI:10.1016/j.jphotochem.2014.04.013

upstream raw materials:

(+)-R-methylisoborneol