CAS 10420-89-0
:(-)-1-(1-Naftil)etilamina
Descripción:
(-)-1-(1-Naftil)etilamina, con el número CAS 10420-89-0, es un compuesto orgánico caracterizado por su grupo funcional amina y un sustituyente naftilo. Este compuesto presenta un centro quiral, lo que contribuye a sus propiedades enantioméricas, con la designación "(-)" que indica su estereoequilibrio específico. Típicamente es un líquido o sólido incoloro a amarillo pálido, dependiendo de la temperatura y la pureza. La presencia del grupo naftilo confiere características hidrofóbicas significativas, influyendo en su solubilidad en disolventes orgánicos mientras lo hace menos soluble en agua. Este compuesto se utiliza a menudo en síntesis orgánica y como bloque de construcción en el desarrollo de productos farmacéuticos y agroquímicos. Su actividad biológica puede incluir interacciones con varios receptores, lo que lo hace de interés en la química medicinal. Se deben consultar los datos de seguridad para su manejo, ya que las aminas pueden ser irritantes y pueden representar riesgos para la salud si no se gestionan adecuadamente. En general, (-)-1-(1-Naftil)etilamina es un compuesto valioso tanto en aplicaciones de investigación como industriales.
Fórmula:C12H13N
InChI:InChI=1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3/t9-/m0/s1
Clave InChI:InChIKey=RTCUCQWIICFPOD-VIFPVBQESA-N
SMILES:[C@@H](C)(N)C=1C2=C(C=CC1)C=CC=C2
Sinónimos:- (-)-1-(1-Naphthyl)ethylamine
- (-)-1-(α-Naphthyl)ethylamine
- (-)-[(S)-1-(1-Naphthyl)ethyl]amine
- (-)-α-(1-Naphthyl)ethylamine
- (1R)-1-naphthalen-1-ylethanamine
- (1S)-1-(1-Naphthyl)ethanamine
- (1S)-1-(1-Naphthyl)ethylamine
- (1S)-1-(naphthalen-1-yl)ethan-1-amine
- (1S)-1-Naphthalen-1-Ylethanamine
- (1S)-1-naphthalen-1-ylethanaminium
- (S)(-)-Alpha-(1-Naphthyl)Ethylamine
- (S)- (+)-α-(1-Naphthyl)ethylamine
- (S)-(-)-(1-Naphthyl)ethylamine
- (S)-(-)-1-(α-Naphthyl)ethylamine
- (S)-(-)-Alpha-(1-Aminoethyl)Naphthalene
- (S)-1-(Naphthalen-1-Yl)Ethanamine
- (S)-1-Naphthylethylamine
- (S)-α-Methyl-1-naphthalenemethanamine
- (S)-α-Naphthylethylamine
- (αS)-α-Methyl-1-naphthalenemethanamine
- 1-Naphthalenemethanamine, α-methyl-, (S)-
- 1-Naphthalenemethanamine, α-methyl-, (αS)-
- 1-Naphthalenemethylamine, α-methyl-, (S)-(-)-
- L-A-(1-Naphthyl)Ethylamine
- L-Alpha-(Alpha-Naphthyl)Ethylamine
- [(S)-1-(Naphthalen-1-yl)ethyl]amine
- Ver más sinónimos
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Encontrado 9 productos.
(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Fórmula:C12H13NPureza:>99.0%(GC)Forma y color:Colorless to Light orange to Yellow clear liquidPeso molecular:171.24(S)-(-)-1-(1-Naphthyl)ethylamine, 99%
CAS:<p>(S)-(-)-1-(1-Naphthyl)ethylamine, (S)-(-)-1-(1-Naphthyl)ethylamine is used in the asymmetric synthesis of -cyanocarboxylates. Also used in the synthesis of chiral imadazolin-2-ylidene ligands used in organometallic catalysis. Chiral/Asymmetric synthesis. This Thermo Scientific Chemicals brand produc</p>Fórmula:C12H14NPureza:99%Forma y color:Clear colorless to yellow, LiquidPeso molecular:172.25(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Fórmula:C12H13NPureza:98%Forma y color:LiquidPeso molecular:171.23831-[(1S)-1-Aminoethyl]naphthalene
CAS:<p>1-[(1S)-1-Aminoethyl]naphthalene</p>Fórmula:C12H13NPureza:97%Forma y color: yellow liquidPeso molecular:171.24g/mol(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Producto controlado<p>Applications (S)-(-)-1-(1-Naphthyl)ethylamine is used in the asymmetric synthesis of α-cyanocarboxylates. Also used in the synthesis of chiral imadazolin-2-ylidene ligands used in organometallic catalysis. Chiral/Asymmetric synthesis.<br>References Herrmann, W. et al.: Organometal., 16, 2472 (1997); Martin, F. et al.: 121, 5467 (1999); Sawamura, M. et al.: J. Am. Chem. Soc., 114, 8295 (1992);<br></p>Fórmula:C12H13NForma y color:NeatPeso molecular:171.24(S)-(-)-1-(1-Naphthyl)ethyl amine
CAS:<p>(S)-(-)-1-(1-Naphthyl)ethyl amine is a chromatographic stationary phase that is used in the separation of fatty acids. It consists of an amine group bound to a naphthalene ring, which is tethered to a long alkyl chain. The stationary phase can be immobilized on silica gel or other solid support matrixes and is useful for analyzing fatty acids. This stationary phase can also be used as a model system to study the interactions between fatty acid molecules and other compounds. The enantiomers (R)-(+)-1-(1-naphthyl)ethyl amine and (S)-(-)-1-(1-naphthyl)ethyl amine are available. Although these two compounds are homologues, they have different physical properties, such as boiling points and melting points. Using an analytical method called high performance liquid chromatography (HPLC), it is possible to separate these two enantiomer</p>Fórmula:C12H13NPureza:Min. 95%Forma y color:Slightly Yellow Clear LiquidPeso molecular:171.24 g/mol(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Fórmula:C12H13NPureza:98%Forma y color:Liquid, Dense light orange liquidPeso molecular:171.243








