2-(4-Nitrophenyl)ethylamine hydrochloride, 98+%, Thermo Scientific Chemicals
2-(4-Nitrophenyl)ethylamine hydrochloride, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-(4-Nitrophenyl)ethylamine hydrochloride, 98+%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
1 g
5 g
Catalog number H64894.14
also known as H64894-14
Price (USD)/ Each
340.65
Online exclusive
378.00 
Save 37.35 (10%)
-
Add to cart
Quantity:
25 g
Request bulk or custom format
Price (USD)/ Each
340.65
Online exclusive
378.00 
Save 37.35 (10%)
Add to cart
2-(4-Nitrophenyl)ethylamine hydrochloride, 98+%, Thermo Scientific Chemicals
Catalog numberH64894.14
Price (USD)/ Each
340.65
Online exclusive
378.00 
Save 37.35 (10%)
-
Add to cart
Chemical Identifiers
CAS29968-78-3
IUPAC Name2-(4-nitrophenyl)ethan-1-aminium
Molecular FormulaC8H11N2O2
InChI KeyIOXOZOPLBFXYLM-UHFFFAOYSA-O
SMILES[NH3+]CCC1=CC=C(C=C1)[N+]([O-])=O
View more
SpecificationsSpecification SheetSpecification Sheet
Assay (HPLC)>98.0%
4-Nitrophenethylamine hydrochloride was used in the synthesis of ortho-metalated primary phenethylamines complexes containing six-membered palladacycles and N-(4-nitrophenethyl)formamide.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Nitrophenethylamine hydrochloride was used in the synthesis of ortho-metalated primary phenethylamines complexes containing six-membered palladacycles and N-(4-nitrophenethyl)formamide.

Solubility
Soluble in methanol almost transparency.

Notes
Store in cool, dry place in tightly closed container. With adequate ventilation. Store away from oxidizing agent.
RUO – Research Use Only

General References:

  1. Vicente J, et al. Ortho-metalated primary amines. 6.1 The first synthesis of six-membered palladacycles from primary amines containing electron-withdrawing substituents: end of the limiting rules of Cope and Friedrich on cyclopalladation of benzyl-and phenethylamines. Organometallics.2003 22(26), 5513-5517.
  2. Tatsuya Maruyama; Kenichi Onda; Masahiko Hayakawa; Tetsuo Matsui; Toshiyuki Takasu; Mitsuaki Ohta. Discovery of novel acetanilide derivatives as potent and selective β3-adrenergic receptor agonists. European Journal of Medicinal Chemistry.2009 44(6), 2533-2543.