CAS 10420-89-0
:(-)-1-(1-Naphthyl)ethylamin
Formel:C12H13N
InChl: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
InChI Key:InChIKey=RTCUCQWIICFPOD-VIFPVBQESA-N
SMILES:[C@@H](C)(N)C=1C2=C(C=CC1)C=CC=C2
Synonyme:- (-)-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
- Weitere Synonyme anzeigen
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10 Produkte gefunden.
(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Formel:C12H13NReinheit:>99.0%(GC)Farbe und Form:Colorless to Light orange to Yellow clear liquidMolekulargewicht:171.24(S)-(-)-1-(1-Naphthyl)ethylamine, 99%
CAS:(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 producFormel:C12H14NReinheit:99%Farbe und Form:Clear colorless to yellow, LiquidMolekulargewicht:172.25(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Formel:C12H13NReinheit:98%Farbe und Form:LiquidMolekulargewicht:171.2383(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:(S)-(-)-1-(1-Naphthyl)ethylamineFormel:C12H13NReinheit:98%Molekulargewicht:171.241-[(1S)-1-Aminoethyl]naphthalene
CAS:1-[(1S)-1-Aminoethyl]naphthaleneFormel:C12H13NReinheit:97%Farbe und Form:LiquidMolekulargewicht:171.23832(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Formel:C12H13NReinheit:98%Farbe und Form:Liquid, Dense light orange liquidMolekulargewicht:171.243(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Kontrolliertes ProduktApplications (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.
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);Formel:C12H13NFarbe und Form:NeatMolekulargewicht:171.24(S)-(-)-1-(1-Naphthyl)ethyl amine
CAS:(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 enantiomerFormel:C12H13NReinheit:Min. 95%Farbe und Form:Slightly Yellow Clear LiquidMolekulargewicht:171.24 g/mol









