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Merck
CN

27350

Sigma-Aldrich

辛可尼丁

purum, ≥98.0% (dried material, NT)

别名:

金鸡尼丁

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关于此项目

经验公式(希尔记法):
C19H22N2O
化学文摘社编号:
分子量:
294.39
Beilstein:
89690
EC 号:
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
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等级

purum

方案

≥98.0% (dried material, NT)

旋光性

[α]20/D −106±4°, c = 1% in ethanol

杂质

≤15% hydrocinchonine (HPLC)
≤5% quinine (HPLC)

灼烧残渣

≤0.1%

缺失

≤1% loss on drying, 110 °C

mp

204-206 °C (lit.)
~205 °C

SMILES字符串

O[C@@H]([C@@H]1C[C@@H]2CCN1C[C@@H]2C=C)c3ccnc4ccccc34

InChI

1S/C19H22N2O/c1-2-13-12-21-10-8-14(13)11-18(21)19(22)16-7-9-20-17-6-4-3-5-15(16)17/h2-7,9,13-14,18-19,22H,1,8,10-12H2/t13-,14-,18-,19+/m0/s1

InChI key

KMPWYEUPVWOPIM-KODHJQJWSA-N

基因信息

human ... CYP2D6(1565)

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1A

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

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Toshifumi Takeuchi et al.
Chemical record (New York, N.Y.), 5(5), 263-275 (2005-10-08)
Molecular imprinting is a template polymerization technique that can easily provide synthetic polymers capable of molecular recognition for given target molecules. In addition to their highly specific recognition ability, we are attempting to introduce signaling functions to molecularly imprinted polymers
Nobutaka Maeda et al.
Journal of the American Chemical Society, 133(49), 19567-19569 (2011-11-17)
An understanding of the chiral site-substrate interaction is a necessary prerequisite for the rational design and development of efficient heterogeneous asymmetric catalysts. For the enantioselective hydrogenation of α-ketoesters on cinchona-modified platinum, it has earlier been proposed that the crucial interaction
Ryan A Olsen et al.
Journal of the American Chemical Society, 128(49), 15594-15595 (2006-12-07)
The protonation of cinchona alkaloids in solution leads to the severe restriction of their internal rotational degrees of freedom and to the locking of the molecule around a specific conformation held in place by a bridging counterion of the acid
Pierrick Nun et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(12), 3773-3779 (2012-02-11)
The asymmetric alkylation of Schiff bases under basic conditions in a ball mill was performed. The starting Schiff bases of glycine were prepared beforehand by milling protected glycine hydrochloride and benzophenone imine, in the absence of solvent. The Schiff base
Simon Diezi et al.
Journal of the American Chemical Society, 128(12), 4048-4057 (2006-03-23)
In the Pt-catalyzed hydrogenation of 1,1,1-trifluoro-2,4-diketones, addition of trace amounts of cinchonidine, O-methyl-cinchonidine, or (R,R)-pantoyl-naphthylethylamine induces up to 93% ee and enhances the chemoselectivity up to 100% in the hydrogenation of the activated carbonyl group to an OH function. A

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