Glicina éster de tert-butilo, 97 %, Thermo Scientific Chemicals
Glicina éster de tert-butilo, 97 %, Thermo Scientific Chemicals
Glicina éster de tert-butilo, 97 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Glicina éster de tert-butilo, 97 %, Thermo Scientific Chemicals

CAS: 6456-74-2 | C6H13NO2 | 131.175 g/mol
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Cantidad:
1 g
5 g
Número de catálogo L16258.06
también denominado L16258-06
Precio (EUR)
248,00
Each
Cantidad:
5 g
Pedido a granel o personalizado
Precio (EUR)
248,00
Each
Identificadores químicos
CAS6456-74-2
IUPAC Nametert-butyl 2-aminoacetate
Molecular FormulaC6H13NO2
InChI KeySJMDMGHPMLKLHQ-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)CN
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)Clear colorless to yellow
Assay (GC)≥95.0%
FormLiquid
Refractive Index1.4215-1.4265 @ 20°C
Glycine tert-butyl ester is used in the preparation of Schiff base by reacting with benzophenone. The resultant Schiff base undergoes asymmetric alkylation with arylmethyl bromides in the presence of O-allyl-N-(9-anthracenylmethyl)cinchonidinium bromide as chiral phase transfer catalyst to give guanidine-containing pentacyclic compound.

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
El éster tert-butilo de glicina se utiliza en la preparación de la base de Schiff reaccionando con benzofenona. La base de Schiff resultante sufre alquilación asimétrica con bromuros de arilmetil en presencia de bromuro de o-alilo-N-(9-antracenilmetil)cinconidinium como catalizador de transferencia de fase quiral para dar compuesto pentacíclico que contiene guanidina.

Solubilidad
Miscible con acetona y metanol. Ligeramente miscible con etanol. Inmiscible con agua.

Notas
Sensible al aire. Almacenar en lugar fresco. Incompatible con agentes oxidantes fuertes.
RUO – Research Use Only

General References:

  1. Lou, S.; Ramirez, A.; Conlon, D. A. Catalytic syn-Selective Direct Aldol Reactions of Benzophenone Glycine Imine with Aromatic, Heteroaromatic and Aliphatic Aldehydes. Adv. Synth. Catal. 2015, 357 (1), 28-34.
  2. Peng, Z.; McLuckey, S. A. C-terminal peptide extension via gas-phase ion/ion reactions. Int. J. Mass Spectrom. 2015, 391, 17-23.