Dibutyl-methyl-tridecylazanium

Base Information

Chemical Name:Dibutyl-methyl-tridecylazanium
CAS No.:6672-74-8
Molecular Formula:C16H14 O2
Molecular Weight:238.286
Hs Code.:
DSSTox Substance ID:DTXSID50409605

Synonyms:6672-74-8;dibutyl-methyl-tridecylazanium;DTXSID50409605

Suppliers and Price of Dibutyl-methyl-tridecylazanium

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 1 raw suppliers

Chemical Property of Dibutyl-methyl-tridecylazanium

Chemical Property:

XLogP3:8.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:18
Exact Mass:326.378675535
Heavy Atom Count:23
Complexity:216

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:CCCCCCCCCCCCC[N+](C)(CCCC)CCCC

Technology Process of Dibutyl-methyl-tridecylazanium

There total 2 articles about Dibutyl-methyl-tridecylazanium 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:

: 855254-83-0
2'-(α-hydroxy-isopropyl)-biphenyl-carboxylic acid-(2)

: 6672-74-8
7,7-dimethyl-7H-dibenzo[c,e]oxepin-5-one

Guidance literature:: With hydrogenchloride; ethanol;

Reference yield:

: 6672-74-8
7,7-dimethyl-7H-dibenzo[c,e]oxepin-5-one

Guidance literature:: aus Diphensaeureanhydrid, Dimethylcadmium;

Reference yield:

: 6672-74-8
7,7-dimethyl-7H-dibenzo[c,e]oxepin-5-one

: 4569-45-3
9,9-dimethyl-9H-fluorene

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous H₂SO₄

2: quinoline; copper-powder

With quinoline; sulfuric acid; copper;
DOI:10.1039/jr9570003477