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Merck
CN
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文件

安全信息

137022

Sigma-Aldrich

1,2-二苯乙胺

97%

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线性分子式:
C6H5CH2CH(C6H5)NH2
CAS号:
25611-78-3
分子量:
197.28
EC 号:
247-126-4
MDL编号:
MFCD00008063
UNSPSC代码:
12352100
PubChem化学物质编号:
24848307
NACRES:
NA.22

产品线

EMPROVE® Bio

检测方案

97%

形式

liquid

折射率

n20/D 1.58 (lit.)

bp

310-311 °C/750 mmHg (lit.)

密度

1.02 g/mL at 25 °C (lit.)

SMILES字符串

NC(Cc1ccccc1)c2ccccc2

InChI

1S/C14H15N/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10,14H,11,15H2

InChI key

DTGGNTMERRTPLR-UHFFFAOYSA-N

一般描述

(S)- and (R)-enantiomers of 1,2-diphenylethylamine are the precursors for synthesis of (S)- and (R)-1-(1,2-diphenylethyl)piperidine.

法律信息

Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

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

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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Michael L Berger et al.
Bioorganic & medicinal chemistry, 17(9), 3456-3462 (2009-04-07)
We resolved 1,2-diphenylethylamine (DPEA) into its (S)- and (R)-enantiomer and used them as precursors for synthesis of (S)- and (R)-1-(1,2-diphenylethyl)piperidine, flexible homeomorphs of the NMDA channel blocker MK-801. We also describe the synthesis of the dicyclohexyl analogues of DPEA. These
Carina S D Wink et al.
Analytical and bioanalytical chemistry, 407(6), 1545-1557 (2015-01-13)
Lefetamine (N,N-dimethyl-1,2-diphenylethylamine, L-SPA) was marketed as an opioid analgesic in Japan and Italy. After being widely abused, it became a controlled substance. It seems to be a pharmaceutical lead for designer drugs because N-ethyl-1,2-diphenylethylamine (NEDPA) and N-iso-propyl-1,2-diphenylethylamine (NPDPA) were confiscated
Daniel A Spudeit et al.
Journal of chromatography. A, 1363, 89-95 (2014-08-30)
This work reports a comparison of HPLC separations of enantiomers with chiral stationary phases (CSPs) prepared by chemically bonding cyclofructan-6, functionalized with isopropyl carbamate groups on fully and superficially porous particles (SPPs). The chromatographic performance of the superficially porous CSP

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