2-(2-Bromophenyl)ethylamine, 97%
2-(2-Bromophenyl)ethylamine, 97%
2-(2-Bromophenyl)ethylamine, 97%
2-(2-Bromophenyl)ethylamine, 97%
Thermo Scientific Chemicals

2-(2-Bromophenyl)ethylamine, 97%

CAS: 65185-58-2 | C8H10BrN | 200.079 g/mol
製品番号(カタログ番号) H60739.09
または、製品番号H60739-09
価格(JPY)
-
見積もりを依頼する
数量:
10 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS65185-58-2
IUPAC Name2-(2-bromophenyl)ethan-1-aminium
Molecular FormulaC8H11BrN
InChI KeyITRNQMJXZUWZQL-UHFFFAOYSA-O
SMILES[NH3+]CCC1=CC=CC=C1Br
さらに表示
Assay (HPLC)>96.0%
2-(2-Bromophenyl)ethylamine is used as a pharmaceutical intermediate.

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
2-(2-Bromophenyl)ethylamine is used as a pharmaceutical intermediate.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Artis Klapars.; Sean Parris.; Kevin W. Anderson.; Stephen L. Buchwald. Synthesis of Medium Ring Nitrogen Heterocycles via a Tandem Copper-Catalyzed C-N Bond Formation-Ring-Expansion Process. J. Am. Chem. Soc. 2004, 126 (11), 3529-3533.
  2. M. V. Mezentseva.; I. S. Nikolaeva.; E. A. Golovanova.; A. N. Fomina. Synthesis and antiviral activity of 2-anilinomethyl derivatives of 5-hydroxyindole. Pharmaceutical Chemistry Journal. 1990, 24 (10), 749-751.