2-[Methyl(3-methylphenyl)amino]ethan-1-ol

Base Information

Chemical Name:2-[Methyl(3-methylphenyl)amino]ethan-1-ol
CAS No.:2933-55-3
Molecular Formula:C10H15 N O
Molecular Weight:165.2322
Hs Code.:2921499090
DSSTox Substance ID:DTXSID30557037
Nikkaji Number:J153.236G
Wikidata:Q82438782
Mol file:2933-55-3.mol

Synonyms:2933-55-3;2-(N,3-dimethylanilino)ethanol;2-[Methyl(3-methylphenyl)amino]ethan-1-ol;3-METHYL-N-METHYL-N-HYDROXYETHYLANILINE;SCHEMBL8095675;DTXSID30557037;RWHHVRRGOAJMNV-UHFFFAOYSA-N;AKOS011263747

Suppliers and Price of 2-[Methyl(3-methylphenyl)amino]ethan-1-ol

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 4 raw suppliers

Chemical Property of 2-[Methyl(3-methylphenyl)amino]ethan-1-ol

Chemical Property:

PSA：23.47000
LogP:1.42350
XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:165.115364102
Heavy Atom Count:12
Complexity:127

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC=C1)N(C)CCO

Technology Process of 2-[Methyl(3-methylphenyl)amino]ethan-1-ol

There total 6 articles about 2-[Methyl(3-methylphenyl)amino]ethan-1-ol 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: 72.0%

: 696-44-6
N-methyl-m-toluidine

: 56-81-5,25618-55-7,64333-26-2,8013-25-0
glycerol

: 2933-55-3
3-methyl-N-methyl-N-hydroxyethylaniline

Guidance literature:: With N-methyl-1-(thiophen-2-yl)methanamine; tris(triphenylphosphine)ruthenium(II) chloride; 1,1'-bis(dicyclohexylphosphinocyclopentadienyl)iron; potassium tert-butylate; In 1,4-dioxane; at 150 ℃; for 20h;
DOI:10.1002/cssc.201903151

Reference yield: 71.0%

: 87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2
D-Xylose

: 696-44-6
N-methyl-m-toluidine

: 2933-55-3
3-methyl-N-methyl-N-hydroxyethylaniline

Guidance literature:: With [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); acetic acid; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; at 150 ℃; for 16h; chemoselective reaction; Inert atmosphere; Glovebox;
DOI:10.1039/c9gc01195a

Reference yield:

: C₁₆H₂₆BNO₂

: 2933-55-3
3-methyl-N-methyl-N-hydroxyethylaniline

Guidance literature:: With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; diethyl ether; water; at 0 - 20 ℃; for 1h; Schlenk technique; Inert atmosphere;
DOI:10.1021/jacs.1c06186