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2-(4-Fluorophenyl)ethylamine, 97%, Thermo Scientific Chemicals
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Catalog number H61791.14
also known as H61791-14
Price (USD)/ Each
61.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
72.80 Save 11.15 (15%)
-
Quantity:
25 g
Price (USD)/ Each
61.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
72.80 Save 11.15 (15%)
2-(4-Fluorophenyl)ethylamine, 97%, Thermo Scientific Chemicals
Catalog numberH61791.14
Price (USD)/ Each
61.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
72.80 Save 11.15 (15%)
-
Chemical Identifiers
CAS1583-88-6
IUPAC Name2-(4-fluorophenyl)ethan-1-aminium
Molecular FormulaC8H11FN
InChI KeyCKLFJWXRWIQYOC-UHFFFAOYSA-O
SMILES[NH3+]CCC1=CC=C(F)C=C1
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Specifications
Specification Sheet
Specification SheetAssay (GC)>96.0%
2-(4-Fluorophenyl)ethylamine may be employed as nucleophile in the synthesis of 2-amino-4-arylpyrimidine derivatives. It is suitable for use in the preparation of ortho-metalated primary phenethylamines having electron-releasing and electron-withdrawing groups on the aromatic ring, leading to complexes containing six membered palladacycles.
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-(4-Fluorophenyl)ethylamine may be employed as nucleophile in the synthesis of 2-amino-4-arylpyrimidine derivatives. It is suitable for use in the preparation of ortho-metalated primary phenethylamines having electron-releasing and electron-withdrawing groups on the aromatic ring, leading to complexes containing six membered palladacycles.
Solubility
Slightly soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents and acids.
2-(4-Fluorophenyl)ethylamine may be employed as nucleophile in the synthesis of 2-amino-4-arylpyrimidine derivatives. It is suitable for use in the preparation of ortho-metalated primary phenethylamines having electron-releasing and electron-withdrawing groups on the aromatic ring, leading to complexes containing six membered palladacycles.
Solubility
Slightly soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents and acids.
RUO – Research Use Only
General References:
- Mitra Matloobi; C.Oliver Kappe. Microwave-assisted solution- and solid-phase synthesis of 2-amino-4-arylpyrimidine derivatives. Journal of Combinatorial Chemistry. 2007, 9,(2), 275-284.
- Jose Vicente; Isabel Saura-Llamas; Jesus Cuadrado; Carmen Ramirez de Arellano. 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.