N-(1-phenylethyl)propan-2-amine

Base Information

Chemical Name:N-(1-phenylethyl)propan-2-amine
CAS No.:19302-16-0
Molecular Formula:C11H17N
Molecular Weight:163.263
Hs Code.:2921499090
European Community (EC) Number:874-324-3
DSSTox Substance ID:DTXSID10396683
Nikkaji Number:J1.112.151I
Mol file:19302-16-0.mol

Synonyms:N-(1-phenylethyl)propan-2-amine;19302-16-0;(1-phenylethyl)(propan-2-yl)amine;SCHEMBL278474;DTXSID10396683;Isopropyl(alpha-methylbenzyl)amine;AMY10567;AKOS000228626;AKOS016842423;N-isopropyl-(+/-)--methylbenzylamine;CS-0312298;FT-0768371;EN300-162761;L10160;A813624

Suppliers and Price of N-(1-phenylethyl)propan-2-amine

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-phenylethyl)propan-2-amine
1g
$ 175.00

Crysdot
N-(1-Phenylethyl)propan-2-amine 95+%
1g
$ 353.00

American Custom Chemicals Corporation
(1-PHENYLETHYL)(PROPAN-2-YL)AMINE 95.00%
5MG
$ 499.33

Alichem
N-(1-Phenylethyl)propan-2-amine
1g
$ 293.76

AK Scientific
N-(1-Phenylethyl)propan-2-amine
100mg
$ 181.00

Total 20 raw suppliers

Chemical Property of N-(1-phenylethyl)propan-2-amine

Chemical Property:

Boiling Point:215℃
PKA:9.77±0.29(Predicted)
Flash Point:77℃
PSA：12.03000
Density:0.898
LogP:3.13650
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:163.136099547
Heavy Atom Count:12
Complexity:114

Purity/Quality:

97% ^*data from raw suppliers

N-(1-phenylethyl)propan-2-amine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)NC(C)C1=CC=CC=C1

Technology Process of N-(1-phenylethyl)propan-2-amine

There total 19 articles about N-(1-phenylethyl)propan-2-amine 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: 98.0%

: 108-18-9
diisopropylamine

: 618-36-0
rac-methylbenzylamine

: 19302-16-0
N-isopropyl-(+/-)-α-methylbenzylamine

Guidance literature:: With μ-diiodo-di((η5-pentamethylcyclopentadienyl)(iodo)iridium); In 5,5-dimethyl-1,3-cyclohexadiene; at 155 ℃; for 10h; Inert atmosphere;
DOI:10.1002/anie.200904028

Reference yield: 91.0%

: 67-63-0,8013-70-5
isopropyl alcohol

: 618-36-0
rac-methylbenzylamine

: 19302-16-0
N-isopropyl-(+/-)-α-methylbenzylamine

Guidance literature:: With μ-diiodo-di((η5-pentamethylcyclopentadienyl)(iodo)iridium); In water; at 115 ℃; for 10h; Inert atmosphere;
DOI:10.1039/b923083a

Reference yield: 83.0%

: 75-31-0
isopropylamine

: 98-86-2
acetophenone

: 19302-16-0
N-isopropyl-(+/-)-α-methylbenzylamine

Guidance literature:: isopropylamine; acetophenone; With titanium tetrachloride; In dichloromethane; at 20 ℃; for 3h;

With sodium cyanoborohydride; In methanol; dichloromethane; at 20 ℃; for 1h;
DOI:10.1039/b403481c