CAS 10420-89-0
:(-)-1-(1-Naphthyl)ethylamine
Formula: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
InChI key:InChIKey=RTCUCQWIICFPOD-VIFPVBQESA-N
SMILES:[C@@H](C)(N)C=1C2=C(C=CC1)C=CC=C2
Synonyms:- (-)-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
- See more synonyms
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Found 10 products.
(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Formula:C12H13NPurity:>99.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight: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 producFormula:C12H14NPurity:99%Color and Shape:Clear colorless to yellow, LiquidMolecular weight:172.25(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Formula:C12H13NPurity:98%Color and Shape:LiquidMolecular weight:171.2383(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:(S)-(-)-1-(1-Naphthyl)ethylamineFormula:C12H13NPurity:98%Molecular weight:171.241-[(1S)-1-Aminoethyl]naphthalene
CAS:1-[(1S)-1-Aminoethyl]naphthaleneFormula:C12H13NPurity:97%Color and Shape:LiquidMolecular weight:171.23832(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Formula:C12H13NPurity:98%Color and Shape:Liquid, Dense light orange liquidMolecular weight:171.243(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Controlled ProductApplications (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);Formula:C12H13NColor and Shape:NeatMolecular weight: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 enantiomerFormula:C12H13NPurity:Min. 95%Color and Shape:Slightly Yellow Clear LiquidMolecular weight:171.24 g/mol









