2-Methyl-N-(2-methylprop-2-en-1-yl)aniline

Base Information

Chemical Name:2-Methyl-N-(2-methylprop-2-en-1-yl)aniline
CAS No.:131001-34-8
Molecular Formula:C11H15N
Molecular Weight:161.247
Hs Code.:
DSSTox Substance ID:DTXSID40563785
Nikkaji Number:J475.413A
Wikidata:Q82448271

Synonyms:131001-34-8;2-Methyl-N-(2-methylprop-2-en-1-yl)aniline;DTXSID40563785;AKOS009049598

Suppliers and Price of 2-Methyl-N-(2-methylprop-2-en-1-yl)aniline

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 2-Methyl-N-(2-methylprop-2-en-1-yl)aniline

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:161.120449483
Heavy Atom Count:12
Complexity:151

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:CC1=CC=CC=C1NCC(=C)C

Technology Process of 2-Methyl-N-(2-methylprop-2-en-1-yl)aniline

There total 1 articles about 2-Methyl-N-(2-methylprop-2-en-1-yl)aniline 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:

: 88-72-2
1-methyl-2-nitrobenzene

: 5674-01-1
2-methylallylmagnesium chloride

: 131001-34-8
N-Methallyl-o-toluidine

: 131001-33-7
N-Methallyl-N-(o-tolyl)hydroxylamine

Guidance literature:: With lithium aluminium tetrahydride; palladium on activated charcoal; Yield given. Multistep reaction. Yields of byproduct given; 1) THF, -70 deg C, 20 min, 2) 20 deg C, 20 min;

Reference yield: 30.0%

: 201230-82-2
carbon monoxide

: 131001-34-8
N-Methallyl-o-toluidine

: 139944-70-0
N-(isobutyl)-2-methylaniline

: 139944-64-2
3-Methyl-1-o-tolyl-pyrrolidine

Guidance literature:: With sodium tetrahydroborate; η⁶-C6H6BPh3^-Rh(COD)⁺; In dichloromethane; isopropyl alcohol; at 100 ℃; for 30h; under 26220 Torr;
DOI:10.1021/jo00038a019