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137022

1,2-二苯乙胺

Name: 1,2-二苯乙胺
Brand: ALDRICH

97%

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About This Item

線性公式:

C₆H₅CH₂CH(C₆H₅)NH₂

CAS號碼:

25611-78-3

分子量：:

197.28

EC號碼:

247-126-4

MDL號碼:

MFCD00008063

分類程式碼代碼:

12352100

PubChem物質ID:

24848307

NACRES:

NA.22

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產品線

EMPROVE^® Bio

化驗

97%

形狀

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 密鑰

DTGGNTMERRTPLR-UHFFFAOYSA-N

一般說明

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

法律資訊

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

象形圖

GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

防範說明

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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分析證明 (COA)

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NMDA receptor affinities of 1,2-diphenylethylamine and 1-(1,2-diphenylethyl)piperidine enantiomers and of related compounds.

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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

Lefetamine, a controlled drug and pharmaceutical lead of new designer drugs: synthesis, metabolism, and detectability in urine and human liver preparations using GC-MS, LC-MS(n), and LC-high resolution-MS/MS.

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

Superficially porous particles vs. fully porous particles for bonded high performance liquid chromatographic chiral stationary phases: isopropyl cyclofructan 6.

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

我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.

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重要文件

1,2-二苯乙胺

97%

About This Item

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屬性

產品線

化驗

形狀

折射率

bp

密度

SMILES 字串

InChI

InChI 密鑰

描述

一般說明

法律資訊

安全資訊

象形圖

訊號詞

危險聲明

防範說明

危險分類

標靶器官

儲存類別代碼

水污染物質分類（WGK）

閃點（°F）

閃點（°C）

個人防護裝備

文件

分析證明 (COA)

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