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3886-69-9 - (R)-(+)-1-Phenylethylamine, ChiPros 99+%, ee 99+% - D-(+)-alpha-Methylbenzylamine - L19117 - Alfa Aesar

L19117 (R)-(+)-1-Phenylethylamine, ChiPros 99+%, ee 99+%

Número CAS
3886-69-9
Nombre Alternativo
D-(+)-alpha-Methylbenzylamine

Tamaño Precio ($) Cantidad Disponibilidad
5g 24,30
25g 52,70
100g 138,00
Añadir al carrito Añadir al presupuesto al por mayor Ver artículo

(R)-(+)-1-Phenylethylamine, ChiPros 99+%, ee 99+%

MDL
MFCD00064405
EINECS
223-423-4

Propiedades químicas

Fórmula
C8H11N
Peso molecular
121.18
Punto de fusión
-10°
Punto de ebullición
187°
Punto de inflamabilidad
71°(159°F)
Densidad
0.948
Índice de refracción
1.5260
Sensibilidad
Air Sensitive
Solubilidad
Miscible with water and chloroform.

Aplicaciones

(R)-(+)-1-Phenylethylamine is used as an intermediate in organic synthesis. It is also used to determine the enantiomeric purity of acids.

Notas

Store in a cool place. Air Sensitive. Incompatible with acids, acid chlorides, acid anhydrides, strong oxidizing agents and carbon dioxide.

Referencias documentales

Both enantiomers are widely used resolving agent for chiral acids. They also find extensive use as chiral auxiliaries in asymmetric synthesis:

For use in the enantioselective synthesis of ɑ-amino nitriles and amino acids in the Strecker reaction, see: Chem. Ber., 110, 2098 (1977); J. Org. Chem., 48, 5369 (1983). Similarly, the preformed imines can be reacted with Trimethyl­silyl­ cyanide, A19598: Chem. Lett., 331, 737 (1975). Enantioselective synthesis of cyclohexylamines from 2-alkylcyclohexanones via the imine and reduction: Tetrahedron Lett., 22, 2633 (1981); Chem. Ber., 117, 2076 (1984). Enantioselective synthesis of ɑ-aminoacetals from 1,1-dialkoxy-2-propanones: Synthesis, 608 (1989).

Selivanova, S. V.; Toscano, A.; Abate, C.; Berardi, F.; Müller, A.; Krämer, S. D.; Schibli, R.; Ametamey, S. M. Synthesis and pharmacological evaluation of 11C-labeled piperazine derivative as a PET probe for sigma-2 receptor imaging. Nucl. Med. Biol. 2015, 42 (4), 399-405.

Alvarado-Beltrán, I.; Maerten, E.; Toscano, R. A.; López-Cortés, J. G.; Baceiredo, A.; Álvarez-Toledano, C. Enantioselective synthesis of 4-alkenoic acids via Pd-catalyzed allylic alkylation: stereocontrolled construction of gamma and delta-lactones. Tetrahedron: Asymmetry 2015, 26 (15-16), 802-809.

Indicaciones de peligro y de precaución del GHS

Indicaciones de peligro (UE): H311-H302-H314-H318-H227

Toxic in contact with skin. Harmful if swallowed. Causes severe skin burns and eye damage. Causes serious eye damage. Combustible liquid.

Indicaciones de precaución: P210-P260-P280-P303+P361+P353-P305+P351+P338-P361-P301+P330+P331-P304+P340-P405-P501a

Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Do not breathe dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Otras referencias

Merck
14,6026
Beilstein
2410916
Clase de peligro
8
Grupo de embalaje
II
Código de tarifa arancelaria unificado
2921.49
TSCA
Yes

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