2,6-Dimethyl-2,5-heptadiene

Base Information

• Chemical Name: 2,6-Dimethyl-2,5-heptadiene
• CAS No.: 6090-16-0
• Molecular Formula: C9H16
• Molecular Weight: 124.226
• Mol file: 6090-16-0.mol

Synonyms:2,6-Dimethyl-2,5-heptadiene

Chemical Property of 2,6-Dimethyl-2,5-heptadiene

Chemical Property:

• PSA: 0.00000
• LogP: 3.30890

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2,6-Dimethyl-2,5-heptadiene

There total 7 articles about 2,6-Dimethyl-2,5-heptadiene 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: 26.0%

2,6-dimethylhept-5-en-2-ol (6090-15-9) → 2,6-dimethyl-2,5-heptadiene (6090-16-0) + 2,6-dimethyl-hepta-1,5-diene (6709-39-3)

Guidance literature:

With pyridine; thionyl chloride; In benzene; at 0 - 20 ℃;

DOI:10.1016/S0040-4039(00)85700-7

Reference yield:

2,2,6,6-tetramethyl-3,4,5,6-tetrahydro-(2H)-pyran (77887-46-8) → 2,6-dimethyl-2,5-heptadiene (6090-16-0) + 2,6-dimethyl-hepta-1,5-diene (6709-39-3)

Guidance literature:

With γ-Al2O3; at 200 ℃; flow reactor;

DOI:10.1016/S0040-4020(01)89939-7

Reference yield:

6-chloro-2,6-dimethyl-hept-2-ene (6076-48-8) → 2,6-dimethyl-2,5-heptadiene (6090-16-0) + 2,6-dimethyl-hepta-1,5-diene (6709-39-3)

Guidance literature:

With pyridine; at 140 ℃;

upstream raw materials:

6-chloro-2,6-dimethyl-hept-2-ene

6-bromo-2,6-dimethyl-n-hept-2-ene

acetic acid-(1,1,5-trimethyl-hex-4-enyl ester)

2,2,6,6-tetramethyl-3,4,5,6-tetrahydro-(2H)-pyran

Refernces

• 1、 Carless, Howard A.J.,Batten, Richard J.. "THE FORMATION AND SUBSEQUENT CYCLISATION OF NOVEL HYDROPEROXIDES FROM A 1,4- AND A 1,5-DIENE". . p. 4735 - 4738. Retrieved 2007/10/02.