2-Propen-1-amine, N-(1,1-dimethylethyl)-

Base Information

Chemical Name:2-Propen-1-amine, N-(1,1-dimethylethyl)-
CAS No.:16486-68-3
Molecular Formula:C7H15N
Molecular Weight:113.20100
Hs Code.:2921199990
Mol file:16486-68-3.mol

Synonyms:2-Propen-1-amine,N-(1,1-dimethylethyl);N-tert-Butylallylamine;N-(1,1-dimethylethyl)-2-propen-1-amine;N-Tert.-butyl-N-(2-propenyl)amine;allyl-tert-butyl-amine;N-tert-butylprop-2-en-1-amine;N-t-butylallylamine;tert-butylallylamine;N-Allyl-N-tert-butylamine;N-(tert-Butyl)-2-propen-1-amine;

Suppliers and Price of 2-Propen-1-amine, N-(1,1-dimethylethyl)-

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

TRC
N-?(1,?1-?dimethylethyl)?-2-?Propen-?1-?amine
50mg
$ 45.00

TCI Chemical
N-Allyl-N-tert-butylamine >98.0%(GC)(T)
100g
$ 435.00

TCI Chemical
N-Allyl-N-tert-butylamine >98.0%(GC)(T)
25g
$ 146.00

AK Scientific
N-Allyl-N-tert-butylamine
5g
$ 112.00

Total 13 raw suppliers

Chemical Property of 2-Propen-1-amine, N-(1,1-dimethylethyl)-

Chemical Property:

Refractive Index:1.4180-1.4200
Boiling Point:112°C(lit.)
PKA:9.91±0.29(Predicted)
PSA：12.03000
Density:0.764±0.06 g/cm3(Predicted)
LogP:1.95140

Purity/Quality:

98% ^*data from raw suppliers

N-?(1,?1-?dimethylethyl)?-2-?Propen-?1-?amine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses N-?(1,?1-?dimethylethyl)?-2-?Propen-?1-?amine has been used in the synthesis of new spiro-?isoquinolinones1 and monoazabutadiene2 due to its secondary N-?allylamines.

Technology Process of 2-Propen-1-amine, N-(1,1-dimethylethyl)-

There total 9 articles about 2-Propen-1-amine, N-(1,1-dimethylethyl)- 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: 82.0%

: 75-64-9
tert-butylamine

: 106-95-6
allyl bromide

: 16486-68-3
N-allyl(tert-butyl)amine

Guidance literature:: at 0 - 20 ℃; for 19h; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.organomet.5b00065

Reference yield: 68.0%

: 845464-89-3
1-(2-allyloxyphenyl)hept-2-yn-1-ol

: 201230-82-2
carbon monoxide

: 75-64-9
tert-butylamine

: 2-(benzofuran-2-yl)hexanoic acid t-butylamide

: 16486-68-3
N-allyl(tert-butyl)amine

Guidance literature:: With triphenylphosphine; potassium iodide; palladium(II) iodide; In acetonitrile; at 100 ℃; for 24h; under 22801.5 Torr;
DOI:10.1021/jo701956k