(R)-(-)-2-Fenilglicinol, 98 %, Thermo Scientific Chemicals
(R)-(-)-2-Fenilglicinol, 98 %, Thermo Scientific Chemicals
(R)-(-)-2-Fenilglicinol, 98 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

(R)-(-)-2-Fenilglicinol, 98 %, Thermo Scientific Chemicals

CAS: 56613-80-0 | C8H12NO | 138.19 g/mol
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Cantidad:
1 g
5 g
25 g
Número de catálogo A19030.14
también denominado A19030-14
Precio (EUR)
350,00
Each
Cantidad:
25 g
Pedido a granel o personalizado
Precio (EUR)
350,00
Each
Identificadores químicos
CAS56613-80-0
IUPAC Name(1S)-2-hydroxy-1-phenylethan-1-aminium
Molecular FormulaC8H12NO
InChI KeyIJXJGQCXFSSHNL-MRVPVSSYSA-O
SMILES[NH3+][C@H](CO)C1=CC=CC=C1
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)White to cream to yellow
Assay (HPLC)≥97.5%
Optical Rotation-30.5 ± 2.5? (C=1.0 in 1N HCl)
FormCrystals or powder or crystalline powder
Melting Point (clear melt)74.0-81.0?C
Amino alcohol used to prepare a chiral imine or oxazolidine from ethyl trifluoropyruvate. These intermediates were then employed in a synthesis of both enantiomers of α-trifluoromethylproline. Chiral β-amino alcohol used as a synthetic building block.

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.

Aplicaciones
Aminoalcohol utilizado para preparar una imina quiral o oxazolidina a partir de trifluoropiruvato de etilo. Estos intermediarios se emplearon en una síntesis de ambos enantiómeros de α-trifluorometilprolina. β-Aminoalcohol quiral usado como bloque de construcción sintético.

Solubilidad
Ligeramente soluble en agua.

Notas
Almacenar en un lugar fresco. Mantenga el recipiente bien cerrado en un lugar seco y bien ventilado. Almacenar lejos de los agentes oxidantes fuertes.
RUO – Research Use Only

General References:

  1. Grégory Chaume et. al. Straightforward synthesis of (S)- and (R)-alpha-trifluoromethyl proline from chiral oxazolidines derived from ethyl trifluoropyruvate.. Organic Letters. 2006, 8 (26), 6123-6126.
  2. Amberley S. Anslow,; Laurence M. Harwood,; Helen Phillips,; David Watkib .Development of a chiral stabilised azomethine ylid. A chiral relay system.. Tetrahedron: Asymmetry. year of publication , 2 (3), 169-172.
  3. Condensation with glutaraldehyde gives a useful intermediate in asymmetric synthesis of alkaloids: Org. Synth. Coll., 9, 176 (1998):
  4. Starting material for the enantioselective synthesis of 2,6-disubstituted piperazines: Synthesis, 833 (1996), and for chiral ɑ-amino phosphonates: Org. Synth., 75, 19 (1997).