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294926

Sigma-Aldrich

1-(1-萘基)乙胺

98%

别名:

(±)-1-(1-萘基)乙胺, (±)-α-甲基-1-萘甲胺

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About This Item

线性分子式:
C10H7CH(CH3)NH2
CAS号:
42882-31-5
分子量:
171.24
Beilstein:
3197375
MDL號碼:
MFCD00004014
分類程式碼代碼:
12352100
PubChem物質ID:
24857746
NACRES:
NA.22

化驗

98%

折射率

n20/D 1.621 (lit.)

bp

156 °C/15 mmHg (lit.)

密度

1.063 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

RTCUCQWIICFPOD-UHFFFAOYSA-N

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一般說明

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.

應用

(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.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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分析证书(COA)

Lot/Batch Number
09817ME
17219EE
11127DD
14616PO
05410HY

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1-萘胺 97%

Sigma-Aldrich

N9005

1-萘胺

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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