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Merck
CN

27350

辛可尼丁

purum, ≥98.0% (dried material, NT)

别名:

金鸡尼丁

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经验公式(希尔记法):
C19H22N2O
化学文摘社编号:
分子量:
294.39
EC Number:
207-622-3
UNSPSC Code:
12352005
PubChem Substance ID:
Beilstein/REAXYS Number:
89690
MDL number:
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InChI key

KMPWYEUPVWOPIM-KODHJQJWSA-N

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

SMILES string

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

grade

purum

assay

≥98.0% (dried material, NT)

optical activity

[α]20/D −106±4°, c = 1% in ethanol

impurities

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

ign. residue

≤0.1%

loss

≤1% loss on drying, 110 °C

Gene Information

human ... CYP2D6(1565)

mp

~205 °C

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type N95 (US)

法规信息

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The preparation of stable metal nanoparticles requires a strong interaction between the (organic) stabilizer and the metal surface that might alter the catalytic properties. This behavior has been described as "poisoning" since the stabilizer normally decreases the catalytic activity due
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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
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
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
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

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