2,3-dimethylhexadecane

Base Information

Chemical Name:2,3-dimethylhexadecane
CAS No.:61868-02-8
Molecular Formula:C₁₈H₃₈
Molecular Weight:254.5
Hs Code.:

Synonyms:

Suppliers and Price of 2,3-dimethylhexadecane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2,3-dimethylhexadecane

Chemical Property:

Vapor Pressure:0.000964mmHg at 25°C

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2,3-dimethylhexadecane

There total 4 articles about 2,3-dimethylhexadecane 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:

: 6803-77-6
Pedicellinsaeure

: 61868-02-8
Pedicellan

Guidance literature:: Multi-step reaction with 3 steps

1: H₂SO₄ / benzene / Heating

2: LiAlH₄ / dimethyl ether / Heating

3: (i) I₂, P, (ii) LiAlH₄, Et₂O

With lithium aluminium tetrahydride; sulfuric acid; In Dimethyl ether; benzene;
DOI:10.1016/S0040-4020(01)99448-7

Reference yield:

: 94874-43-8
2-methyl-3-tridecyl-succinic acid dimethyl ester

: 61868-02-8
Pedicellan

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄ / dimethyl ether / Heating

2: (i) I₂, P, (ii) LiAlH₄, Et₂O

With lithium aluminium tetrahydride; In Dimethyl ether;
DOI:10.1016/S0040-4020(01)99448-7

Reference yield:

: 563-80-4
3-methyl-butan-2-one

: 117711-00-9
tridecylmagnesium bromide

: 61868-02-8
Pedicellan

Guidance literature:: With diethyl ether; und Erhitzen des Reaktionsprodukts mit Naphthalin-2-sulfonsaeure auf 110grad und Hydrieren des erhaltenen Olefin-Gemisches an Raney-Nickel bei 190grad/200 at;