N-(2-AMINOETHYL)-2-(1-NAPHTHYL)ACETAMIDE

Base Information

Chemical Name:N-(2-AMINOETHYL)-2-(1-NAPHTHYL)ACETAMIDE
CAS No.:36321-43-4
Molecular Formula:C14H16 N2 O
Molecular Weight:228.28964
Hs Code.:2924296000
Mol file:36321-43-4.mol

Synonyms:N-(2-Aminoethyl)-1-naphthylacetamide

Suppliers and Price of N-(2-AMINOETHYL)-2-(1-NAPHTHYL)ACETAMIDE

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-(2-Aminoethyl)-1-naphthylacetamide
100mg
$ 185.00

Sigma-Aldrich
Naphazoline impurity A
30mg
$ 1260.00

Sigma-Aldrich
Naphazoline Related Compound A PharmaceuticalSecondaryStandard;CertifiedReferenceMaterial
50MG
$ 499.00

Sigma-Aldrich
Naphazoline impurity A European Pharmacopoeia (EP) Reference Standard
n0200000
$ 190.00

American Custom Chemicals Corporation
N-(2-AMINOETHYL)-1-NAPHTHALENEACETAMIDE 95.00%
5MG
$ 501.44

Acrotein
N-(2-Aminoethyl)-1-naphthaleneacetamide 97%
5g
$ 660.00

Total 14 raw suppliers

Chemical Property of N-(2-AMINOETHYL)-2-(1-NAPHTHYL)ACETAMIDE

Chemical Property:

Boiling Point:491.7°Cat760mmHg
Flash Point:251.2°C
PSA：58.61000
Density:1.147g/cm³
LogP:2.99780
Storage Temp.:Refrigerator, under inert atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly)

Purity/Quality:

99% ^*data from raw suppliers

N-(2-Aminoethyl)-1-naphthylacetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses N-(2-Aminoethyl)-1-naphthylacetamide is a metabolite of Naphazoline that has been seen to be a strong collector for pyrophyllite.

Technology Process of N-(2-AMINOETHYL)-2-(1-NAPHTHYL)ACETAMIDE

There total 2 articles about N-(2-AMINOETHYL)-2-(1-NAPHTHYL)ACETAMIDE 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: 70.0%

: 86-87-3
naphth-1-yl acetic acid

: 107-15-3,85404-18-8
ethylenediamine

: 36321-43-4
N-(1-naphthylacetyl)ethylenediamine

Guidance literature:: naphth-1-yl acetic acid; With 1-hydroxy-pyrrolidine-2,5-dione; diisopropyl-carbodiimide; In chloroform; at 20 ℃; for 1h;

ethylenediamine; In chloroform; at 0 - 20 ℃;
DOI:10.1016/j.bmc.2013.07.026

Reference yield:

: 835-31-4
naphazoline

: 36321-43-4
N-(1-naphthylacetyl)ethylenediamine

Guidance literature:: With sodium hydroxide;

Reference yield:

: 368866-30-2
C₂₈H₂₈N₂O₄

: 36321-43-4
N-(1-naphthylacetyl)ethylenediamine

: 1453814-67-9
C₄₂H₄₂N₄O₄

Guidance literature:: With benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide; In tetrahydrofuran; at 20 ℃; for 18h;
DOI:10.1016/j.bmc.2013.07.026