CAS 10420-89-0
:(-)-1-(1-Naphtyle)éthylamine
Formule :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
Code InChI :InChIKey=RTCUCQWIICFPOD-VIFPVBQESA-N
SMILES :[C@@H](C)(N)C=1C2=C(C=CC1)C=CC=C2
Synonymes :- (-)-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
- Voir plus de synonymes
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10 produits trouvés.
(S)-(-)-1-(1-Naphthyl)ethylamine
CAS :Formule :C12H13NDegré de pureté :>99.0%(GC)Couleur et forme :Colorless to Light orange to Yellow clear liquidMasse moléculaire :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 producFormule :C12H14NDegré de pureté :99%Couleur et forme :Clear colorless to yellow, LiquidMasse moléculaire :172.25(S)-(-)-1-(1-Naphthyl)ethylamine
CAS :Formule :C12H13NDegré de pureté :98%Couleur et forme :LiquidMasse moléculaire :171.23831-[(1S)-1-Aminoethyl]naphthalene
CAS :1-[(1S)-1-Aminoethyl]naphthaleneFormule :C12H13NDegré de pureté :97%Couleur et forme :LiquidMasse moléculaire :171.23832(S)-(-)-1-(1-Naphthyl)ethylamine
CAS :(S)-(-)-1-(1-Naphthyl)ethylamineFormule :C12H13NDegré de pureté :98%Masse moléculaire :171.24(S)-(-)-1-(1-Naphthyl)ethylamine
CAS :Formule :C12H13NDegré de pureté :98%Couleur et forme :Liquid, Dense light orange liquidMasse moléculaire :171.243(S)-(-)-1-(1-Naphthyl)ethylamine
CAS :Produit contrôléApplications (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);Formule :C12H13NCouleur et forme :NeatMasse moléculaire :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 enantiomerFormule :C12H13NDegré de pureté :Min. 95%Couleur et forme :Slightly Yellow Clear LiquidMasse moléculaire :171.24 g/mol









