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Merck
모든 사진(1)

문서

137022

Sigma-Aldrich

1,2-Diphenylethylamine

97%

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About This Item

Linear Formula:
C6H5CH2CH(C6H5)NH2
CAS Number:
Molecular Weight:
197.28
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

제품 라인

EMPROVE® Bio

분석

97%

형태

liquid

refractive index

n20/D 1.58 (lit.)

bp

310-311 °C/750 mmHg (lit.)

density

1.02 g/mL at 25 °C (lit.)

SMILES string

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

일반 설명

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

법적 정보

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

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

235.4 °F - closed cup

Flash Point (°C)

113 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


시험 성적서(COA)

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문서 라이브러리 방문

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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