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166365 S-(-)-1-(1-Naphthyl)ethylamine CAS: 10420-89-0

Specifications
References
CAS Number
10420-89-0
Grade
Highly Purified
Molecular Formula
C12H13N
Molecular Weight
171.24
EU Commodity Code
38220090
Shipping Temp
RT
Storage Temp
RT/4°C
(αS)-α-Methyl-1-naphthalenemethanamine; (S)-α-Methyl-,1-naphthalenemethanamine; (-)-1-(1-Naphthyl)ethylamine; (-)-1-(α-Naphthyl)ethylamine; (-)-[(S)-1-(1-Naphthyl)ethyl]amine; (-)-α-(1-Naphthyl)ethylamine; (1S)-1-(1-Naphthyl)ethanamine; (S)-(-)-(1-Naphthyl)ethylamine; (S)-(-)-1-(1-Naphthyl)ethylamine; (S)-(-)-1-(α-Naphthyl)ethylamine; (S)-(-)-α-(1-Naphthyl)ethylamine; (S)-1-(1-Naphthyl)ethylamine; (S)-1-(Naphthalen-1-yl)ethanamine; (S)-1-(α-Naphthyl)ethylamine; (S)-1-Naphthylethylamine; (S)-α-(1-Naphthyl)ethylamine; (S)-α-Methyl-1-naphthalenemethanamine; (S)-α-Naphthylethylamine; (αS)-α-Methyl-1-naphthalenemethanamine; [(S)-1-(Naphthalen-1-yl)ethyl]amine; l-α-(1-Naphthyl)ethylamine

(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.

Solubility
Chloroform, Ethanol
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);
USBio References
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