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294926

Sigma-Aldrich

1-(1-Naphthyl)ethylamine

98%

Sinónimos:

(±)-1-(1-Naphthyl)ethylamine, (±)-α-Methyl-1-naphthalenemethylamine

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About This Item

Fórmula lineal:
C10H7CH(CH3)NH2
Número de CAS:
42882-31-5
Peso molecular:
171.24
Beilstein/REAXYS Number:
3197375
MDL number:
MFCD00004014
UNSPSC Code:
12352100
PubChem Substance ID:
24857746
NACRES:
NA.22
assay:
98%

assay

98%

refractive index

n20/D 1.621 (lit.)

bp

156 °C/15 mmHg (lit.)

density

1.063 g/mL at 25 °C (lit.)

SMILES string

CC(N)c1cccc2ccccc12

InChI

1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3

InChI key

RTCUCQWIICFPOD-UHFFFAOYSA-N

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General description

The adsorption of 1-(1-naphthyl)ethylamine on platinum surfaces has been characterized by reflection-absorption infrared spectroscopy and temperature-programmed desorption both under ultrahigh vacuum and in situ from liquid solutions.

Application

(R)1-(1-Naphthyl)ethylamine, a new chiral modifier, has been employed in the enantioselective hydrogenation of ethyl pyruvate to ethyl lactate over 5 wt% Pt/Al2O3.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
09817ME
17219EE
11127DD
02602MQ
01415LS

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Sigma-Aldrich

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Sigma-Aldrich

N9005

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Ilkeun Lee et al.
Journal of the American Chemical Society, 130(44), 14597-14604 (2008-10-14)
The adsorption of 1-(1-naphthyl)ethylamine (NEA) on platinum surfaces has been characterized by reflection-absorption infrared spectroscopy (RAIRS) and temperature-programmed desorption (TPD) both under ultrahigh vacuum and in situ from liquid solutions. The main focus of this study was to identify the
Enantioselective Hydrogenation of Ethyl Pyruvate over Pt/Alumina Modified by (R)-1-(1-Naphthyl) ethylamine Derivatives.
Minder B, et al.
J. Catal., 160(2), 261-268 (1992)
Jian Tang et al.
Analytica chimica acta, 946, 96-103 (2016-11-09)
In this work, a detail study has been performed on the enantioselectivity of per(3-chloro-4-methyl)phenylcarbamate-β-CD clicked chiral stationary phase (CSP) in high-performance liquid chromatography. Both normal phase and polar organic mobile phases have been explored for the enantioseparation of 39 model
Francesc Yraola et al.
Journal of medicinal chemistry, 49(21), 6197-6208 (2006-10-13)
Structure activity relationships for semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 (SSAO/VAP-1) were studied using a library of arylalkylamine substrates, with the aim of contributing to the discovery of more efficient SSAO substrates. Experimental data were contrasted with computational docking studies, thereby

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