CAS 10420-89-0
:(-)-1-(1-Naphthyl)ethylamine
Description:
(-)-1-(1-Naphthyl)ethylamine, with the CAS number 10420-89-0, is an organic compound characterized by its amine functional group and a naphthyl substituent. This compound features a chiral center, which contributes to its enantiomeric properties, with the "(-)" designation indicating its specific stereochemistry. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the naphthyl group imparts significant hydrophobic characteristics, influencing its solubility in organic solvents while rendering it less soluble in water. This compound is often utilized in organic synthesis and as a building block in the development of pharmaceuticals and agrochemicals. Its biological activity may include interactions with various receptors, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as amines can be irritants and may pose health risks if not managed properly. Overall, (-)-1-(1-Naphthyl)ethylamine is a valuable compound in both research and industrial applications.
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 9 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:<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>Formula: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:171.23831-[(1S)-1-Aminoethyl]naphthalene
CAS:<p>1-[(1S)-1-Aminoethyl]naphthalene</p>Formula:C12H13NPurity:97%Color and Shape: yellow liquidMolecular weight:171.24g/mol(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Controlled Product<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>Formula:C12H13NColor and Shape:NeatMolecular weight: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>Formula:C12H13NPurity:Min. 95%Color and Shape:Slightly Yellow Clear LiquidMolecular weight:171.24 g/mol(S)-(-)-1-(1-Naphthyl)ethylamine
CAS:Formula:C12H13NPurity:98%Color and Shape:Liquid, Dense light orange liquidMolecular weight:171.243








