
CAS 71845-20-0
:Benzenamine, 4-(2-phenylethyl)-, hydrochloride (1:1)
Description:
Benzenamine, 4-(2-phenylethyl)-, hydrochloride (1:1), also known as 4-(2-phenylethyl)aniline hydrochloride, is an organic compound characterized by its amine functional group and a phenethyl side chain. It appears as a white to off-white crystalline solid and is soluble in water due to the presence of the hydrochloride salt, which enhances its solubility compared to its free base form. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or other chemical products. Its structure features a benzene ring attached to an amine group and a phenethyl group, which contributes to its chemical reactivity and potential biological activity. As with many amines, it may exhibit basic properties and can participate in various chemical reactions, including acylation and alkylation. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled, and appropriate personal protective equipment should be used.
Formula:C14H16ClN
InChI:InChI=1S/C14H15N.ClH/c15-14-10-8-13(9-11-14)7-6-12-4-2-1-3-5-12;/h1-5,8-11H,6-7,15H2;1H
InChI key:InChIKey=QJWSMOWGHWIWRZ-UHFFFAOYSA-N
SMILES:C(CC1=CC=CC=C1)C2=CC=C(N)C=C2.Cl
Synonyms:- [4-(2-Phenylethyl)phenyl]amine hydrochloride
- Benzenamine, 4-(2-phenylethyl)-, hydrochloride (1:1)
- Aniline, p-phenethyl-, hydrochloride
- Benzenamine, 4-(2-phenylethyl)-, hydrochloride
- 4-phenethylaniline hydrochloride
- [4-(2-PHENYLETHYL)PHENYL]AMINEHYDROCHLORIDE
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
[4-(2-Phenylethyl)phenyl]amine hydrochloride
CAS:Formula:C14H16ClNPurity:97%Color and Shape:SolidMolecular weight:233.73654-Phenethylaniline hydrochloride
CAS:4-Phenethylaniline hydrochloridePurity:97%Molecular weight:233.74g/mol4-Phenethylaniline hydrochloride
CAS:Formula:C14H16ClNPurity:97.0%Color and Shape:SolidMolecular weight:233.74[4-(2-Phenylethyl)phenyl]amine hydrochloride
CAS:<p>This is a novel, selective and efficient catalyst for the synthesis of oxiranes from aldehydes and azides. It has been found to be more chemoselective than other catalysts in this area, and can also be used as a catalyst for the synthesis of vicinal silylated oxirane. The catalyst is prepared by reacting an amine with an aldehyde in the presence of hydroxide.<br>Synlett, 2014, 25(2), pp. 166–168</p>Formula:C14H16ClNPurity:Min. 95%Molecular weight:233.74 g/mol




