N-(2-Methylbut-3-en-2-yl)aniline

Base Information

Chemical Name:N-(2-Methylbut-3-en-2-yl)aniline
CAS No.:60173-64-0
Molecular Formula:C11H15N
Molecular Weight:161.247
Hs Code.:
DSSTox Substance ID:DTXSID10543559
Nikkaji Number:J1.527.620G
Wikidata:Q82420478

Synonyms:N-(2-Methylbut-3-en-2-yl)aniline;60173-64-0;N-(1,1-dimethylprop-2-en-1-yl)aniline;DTXSID10543559;UVXBXESWOBZYAM-UHFFFAOYSA-N

Suppliers and Price of N-(2-Methylbut-3-en-2-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

Usbiological
N-1,1-Dimethylallyl-aniline
100mg
$ 389.00

TRC
N-1,1-Dimethylallyl-aniline
500mg
$ 485.00

Total 0 raw suppliers

Chemical Property of N-(2-Methylbut-3-en-2-yl)aniline

Chemical Property:

PSA：12.03000
LogP:3.13610
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:161.120449483
Heavy Atom Count:12
Complexity:143

Purity/Quality:: N-1,1-Dimethylallyl-aniline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C=C)NC1=CC=CC=C1
Uses N-1,1-Dimethylallyl-aniline is an intermediate in the synthesis of Endophenazine A which is a new phenazine antibiotic isolated from the arthropod associated endosymbiont Streptomyces anulatus and shows antimicrobial activities against Gram-positive bacteria and some filamentous fungi, and herbicidal activity against Lemna minor (duckweed).

Technology Process of N-(2-Methylbut-3-en-2-yl)aniline

There total 21 articles about N-(2-Methylbut-3-en-2-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: 89.0%

: 861216-48-0
tert-butyl 2-methylbut-3-en-2-yl carbonate

: 62-53-3
aniline

: 60173-64-0
N-(1,1-dimethylprop-2-en-1-yl)aniline

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; N,N-dimethyl-formamide; at 60 ℃; for 48h; Inert atmosphere;
DOI:10.1021/jacs.8b01005

Reference yield: 87.0%

: 148952-11-8
2,2,2-Trichloro-acetimidic acid 1,1-dimethyl-allyl ester

: 62-53-3
aniline

: 60173-64-0
N-(1,1-dimethylprop-2-en-1-yl)aniline

Guidance literature:: With di-μ-chlorobis(norbornadiene)dirhodium(I); In tetrahydrofuran; at 25 ℃; for 0.5h; regioselective reaction; Inert atmosphere;
DOI:10.1021/ol202313y