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(S)-(−)-1-(1-Naphthyl)ethylamine

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For Research Use Only | Not For Clinical Use
CATAP10420890
CAS10420-89-0
Structure
MDL NumberMFCD00064179
Molecular Weight171.24
InChI KeyRTCUCQWIICFPOD-VIFPVBQESA-N
REAXYS Number2208024
Description≥99%
Density1.067 g/mL at 20 °C (lit.)
Assay≥99%
BP153 °C/11 mmHg (lit.)
Linear FormulaC10H7CH(CH3)NH2
Refractive Indexn20/D 1.623 (lit.)
Size1G, 5G
1

Aspects of Enantioselective Heterogeneous Catalysis: Structure and Reactivity of (S)-(-)-1-(1-naphthyl)ethylamine on Pt[111]

Jonathan M Bonello, Federico J Williams, Richard M Lambert

J Am Chem Soc. 2003 Mar 5;125(9):2723-9.

PMID: 12603161

1

Effective Guest Inclusion by a 6-O-Modified β-Cyclodextrin Dimer in Organic Solvents

Chizuru Asahara, Takuya Iwamoto, Mitsuru Akashi, Hajime Shigemitsu, Toshiyuki Kida

Chempluschem. 2018 Sep;83(9):868-873.

PMID: 31950682

1

Neutral and Ionic Platinum Compounds Containing a Cyclometallated Chiral Primary Amine: Synthesis, Antitumor Activity, DNA Interaction and Topoisomerase I-cathepsin B Inhibition

Joan Albert, Ramon Bosque, Margarita Crespo, Jaume Granell, Concepción López, Raquel Martín, Asensio González, Anusha Jayaraman, Josefina Quirante, Carme Calvis, Josefa Badía, Laura Baldomà, Mercè Font-Bardia, etc.

Dalton Trans. 2015 Aug 14;44(30):13602-14.

PMID: 26140359

1

Optical Resolution of 1-(1-naphthyl)ethylamine by Its Dicarboxylic Acid Derivatives: Structural Features of the Oxalic Acid Derivative Diastereomeric Salt Pair

Laura Bereczki, Petra Bombicz, József Bálint, Gabriella Egri, József Schindler, György Pokol, Elemér Fogassy, Katalin Marthi

Chirality. 2009 Mar;21(3):331-8.

PMID: 18571802

1

Preparation of Two New Diasteromeric Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid and (R)- Or (S)-1-(1-Naphthyl)ethylamine and Chiral Tethering Group Effect on the Chiral Recognition

Rajalingam Agneeswari, Ji Yeong Sung, Eun Sol Jo, Hee Young Jeon, Vellaiappillai Tamilavan, Myung Ho Hyun

Molecules. 2016 Aug 12;21(8):1051.

PMID: 27529205

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