3,5-Dimethoxy-n,n-dimethylaniline

Base Information

Chemical Name:3,5-Dimethoxy-n,n-dimethylaniline
CAS No.:2570-40-3
Molecular Formula:C10H15NO2
Molecular Weight:181.235
Hs Code.:
DSSTox Substance ID:DTXSID90556021
Nikkaji Number:J1.810.003G
Wikidata:Q82437487
Mol file:2570-40-3.mol

Synonyms:3,5-dimethoxy-n,n-dimethylaniline;2570-40-3;Benzenamine, 3,5-dimethoxy-N,N-dimethyl-;SCHEMBL116727;DTXSID90556021;PQZQVAPKETUXEA-UHFFFAOYSA-N

Suppliers and Price of 3,5-Dimethoxy-n,n-dimethylaniline

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 5 raw suppliers

Chemical Property of 3,5-Dimethoxy-n,n-dimethylaniline

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:181.110278721
Heavy Atom Count:13
Complexity:138

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C1=CC(=CC(=C1)OC)OC

Technology Process of 3,5-Dimethoxy-n,n-dimethylaniline

There total 6 articles about 3,5-Dimethoxy-n,n-dimethylaniline 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: 97.0%

: 7051-16-3
1-chloro-3,5-dimethoxybenzene

: 124-40-3
dimethyl amine

: 2570-40-3
3,5-dimethoxy-N,N-dimethylaniline

Guidance literature:: With [2-(di-tert-butylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-((2-aminoethyl)phenyl)]palladium(II) chloride; lithium hexamethyldisilazane; In tetrahydrofuran; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.tetlet.2009.03.137