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
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货号数量
H60739.09
又称 H60739-09
10 g
货号 H60739.09
又称 H60739-09
价格(CNY)
-
数量:
10 g
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化学标识符
CAS65185-58-2
IUPAC Name2-(2-bromophenyl)ethan-1-aminium
Molecular FormulaC8H11BrN
InChI KeyITRNQMJXZUWZQL-UHFFFAOYSA-O
SMILES[NH3+]CCC1=CC=CC=C1Br
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规格Specification Sheet规格表
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.