(S)-(-)-1-(1-Naphthyl)ethylamine, 99%
(S)-(-)-1-(1-Naphthyl)ethylamine, 99%
(S)-(-)-1-(1-Naphthyl)ethylamine, 99%
Thermo Scientific Chemicals

(S)-(-)-1-(1-Naphthyl)ethylamine, 99%

CAS: 10420-89-0 | C12H14N | 172.25 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
1 g
5 g
Catalog number A17176.06
also known as A17176-06
Price (EUR)
162,00
Each
Quantity:
5 g
Request bulk or custom format
Price (EUR)
162,00
Each
Chemical Identifiers
CAS10420-89-0
IUPAC Name(1S)-1-(naphthalen-1-yl)ethan-1-aminium
Molecular FormulaC12H14N
InChI KeyRTCUCQWIICFPOD-VIFPVBQESA-O
SMILESC[C@H]([NH3+])C1=C2C=CC=CC2=CC=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow
Assay (GC)≥98.0% (non-U.S. specification)
Assay from Suppliers CofA≥98.0% (U.S. specification)
CommentMay darken on storage
CommentSpecification differs for U.S. and non-U.S. material where indicated
View more
(S)-(-)-1-(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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(S)-(-)-1-(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
Soluble in chloroform, ethanol.

Notes
Air Sensitive. Stable under recommended storage conditions. Keep away from acids, acid chlorides, acid anhydrides, oxidizing agents, chloroformates.
RUO – Research Use Only

General References:

  1. JM Bonello.; FJ Williams. Aspects of enantioselective heterogeneous catalysis: Structure and reactivity of (S)-(-)-1-(1-naphthyl) ethylamine on Pt {111}. J. Am. Chem. Soc. 2003125 (9), 2723-2729.
  2. NW Alcock.; JM Brown.; DI Hulmes. Synthesis and resolution of 1-(2-diphenylphosphino-1-naphthyl) isoquinoline; a P N chelating ligand for asymmetric catalysis. Tetrahedron: Asymmetry. 19934 (4), 743-756.