CAS 10420-89-0
:(-)-1-(1-Naftil)etilamina
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
Chave 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
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Foram encontrados 10 produtos.
(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Fórmula:C12H13NPureza:>99.0%(GC)Cor e Forma:Colorless to Light orange to Yellow clear liquidPeso molecular: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 producFórmula:C12H14NPureza:99%Cor e Forma:Clear colorless to yellow, LiquidPeso molecular:172.25(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Fórmula:C12H13NPureza:98%Cor e Forma:LiquidPeso molecular:171.2383(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:(S)-(-)-1-(1-Naphthyl)ethylamineFórmula:C12H13NPureza:98%Peso molecular:171.241-[(1S)-1-Aminoethyl]naphthalene
CAS:1-[(1S)-1-Aminoethyl]naphthaleneFórmula:C12H13NPureza:97%Cor e Forma:LiquidPeso molecular:171.23832(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Fórmula:C12H13NPureza:98%Cor e Forma:Liquid, Dense light orange liquidPeso molecular:171.243(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Produto ControladoApplications (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);Fórmula:C12H13NCor e Forma:NeatPeso molecular: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 enantiomerFórmula:C12H13NPureza:Min. 95%Cor e Forma:Slightly Yellow Clear LiquidPeso molecular:171.24 g/mol









