Product manager: selina zhang; Email: selina@coreychem.com
There are two configurations of 1- (1-naphthyl) ethylamine, namely (S) – (-) -1- (1-naphthyl) ethylamine and (R) -1- (1-naphthyl) ethylamine. Among them, (S) – (-) -1- (1-naphthyl) ethylamine is an efficient solvent for separating acetylated derivatives of amino acids, while (R) -1- (1-naphthyl) ethylamine can not only be used as a solvent, but also as an important pharmaceutical intermediate.
| Product Name | (S)-(-)-1-(1-Naphthyl)ethylamine |
| Synonyms | (1S)-1-NAPHTHALEN-1-YLETHANAMINE;(S)-(-)-1-(1-Naphthyl)ethylamine,ChiPros99+%,ee99+%;(S)-(-)-Alpha-(1-naphtyl)ethylamine,99+%,;(-)-1-[(S)-1-Aminoethyl]naphthalene;(1S)-1-(1-Naphthyl)ethanamine;(S)-α-Methylnaphthalene-1-methanamine;(αS)-α-Methylnaphthalene-1-methanamine;[S,(-)]-α-Methyl-1-naphthalenemethanamine |
| CAS NO | 10420-89-0 |
| Purity | 98% |
| Appearance | Light yellow to yellow (Liquid) |
| MF | C12H13N |
| MW | 171.24 |
| Contact | selina@coreychem.com |
Main Functions / Applications of (S)-(-)-1-(1-Naphthyl)ethylamine (CAS: 10420-89-0)
1) Chiral organic synthesis intermediate
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Used as a key raw material for the preparation of chiral amines, chiral alcohols and heterocyclic compounds.
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Applied in asymmetric synthesis and chiral-induction reactions.
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Serves as a chiral source / structural scaffold in lead-compound design for medicinal chemistry.
2) Pharmaceutical research and API intermediate
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Employed in the construction of optically active drug candidate molecules.
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Used as an intermediate in the structural optimization of bioactive compounds such as anticancer, anti-infective and CNS-active molecules.
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Participates in aminylation, amidation, condensation and substitution reactions to build important functional fragments.
3) Chiral resolution and enantiomer purification
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Can be used as a chiral auxiliary or resolving agent.
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Applied in the resolution and confirmation of racemic compounds and their enantiomers.
4) Ligand and catalysis research (limited applications)
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Serves as a precursor for chiral ligands in certain research systems.
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Used in studies of asymmetric catalysis and stereoselective reaction mechanisms.
Recommendations for similar compounds：
| No. | Product Name | CAS Number |
|---|---|---|
| 1 | (S)-(-)-1-(1-Naphthyl)ethylamine | 10420-89-0 |
| 2 | (R)-(+)-1-(1-Naphthyl)ethylamine | 108220-03-0 |
| 3 | (S)-(+)-1-(2-Naphthyl)ethylamine | 2303-40-4 |
| 4 | (R)-(-)-1-(2-Naphthyl)ethylamine | 2510-71-2 |
| 5 | (S)-α-Methylbenzylamine | 98-83-9 |
| 6 | (R)-α-Methylbenzylamine | 620-02-0 |
| 7 | (S)-1-(p-Tolyl)ethylamine | 7682-76-6 |
| 8 | (S)-1-(3,4-Dimethylphenyl)ethylamine | 110144-40-4 |
| 9 | (S)-Phenylethylamine | 51-41-2 |
| 10 | (R)-Phenylethylamine | 620-03-1 |
| 11 | (S)-1-(Naphthylmethyl)amine | 13297-19-5 |
| 12 | (S)-1-(Naphthyl)propan-1-amine | 76137-06-5 |
Contact us for more information: selina@coreychem.com
