名称和标识符别名信息物化性质相关文献相关产品

氢化辛可宁丁 | 485-64-3

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中文名称：氢化辛可宁丁

英文名称： Cinchamidine

CAS No.： 485-64-3

分子式： C₁₉H₂₄N₂O

分子量： 296.40666

如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击：氢化辛可宁丁结构式

价格行情：氢化辛可宁丁价格

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氢化辛可宁丁的其他展现形式

相关化合物

辛可尼丁

(-)-Cinchonidine

CAS No.：485-71-2
二氢金鸡纳宁

(1S)-((2R,4S,5R)-5-Ethylquinuclidin-2-yl)(quinolin-4-yl)methanol

CAS No.：485-65-4
(8Α,9R)-10,11-氢化奎宁-6',9-二醇

Cinchonan-6',9-diol,10,11-dihydro-, (8a,9R)-

CAS No.：5962-19-6
(9R)-9-hydroxy-1-methylcinchonan-1-ium iodide

CAS No.：73804-28-1
(3xi,8alpha,9S)-9-hydroxy-1-methylcinchonan-1-ium iodide

CAS No.：73804-27-0
9-epi-Cinchonidine

CAS No.：550-54-9

名称和标识符

InChIKey	WFJNHVWTKZUUTR-KODHJQJWSA-N
Inchi	InChI=1S/C19H24N2O/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/h3-7,9,13-14,18-19,22H,2,8,10-12H2,1H3/t13-,14-,18-,19+/m0/s1
SMILES	CC[C@H]1CN2CC[C@H]1C[C@H]2[C@@H](C1=CC=NC2=CC=CC=C12)O

别名信息

- 中文别名 -

(S)-Fmoc-2-氨基-5-[(N'-Pbf-N''-Boc-氨基)-胍基]-戊酸
氢化辛可宁丁

- 英文别名 -

Cinchonan-9-ol,10,11-dihydro-, (8a,9R)-
Cinchamidine
DIHYDROCINCHONIDINE
(-)-CINCHONIDINE
(-)-hydrocinchonidine

(+)-cinchonine
10,11-dihydrocinchonidine
1-Cinchonidine
A-QUINIDINE
chinchonidine
Cinchondine
Cinchonidine
Cinchovatine
hydrocinchonidine
L-CINCHONIDINE

物化性质

实验特性

折射率	1.5600 (estimate)
沸点	438°C (rough estimate)
熔点	230°
比旋光度	D15 -98° (alcohol)
密度	1.0689 (rough estimate)

相关文献

1. Molecular design of chiral quaternary ammonium polymers for asymmetric catalysis applications
Md. Masud Parvez,Naoki Haraguchi,Shinichi Itsuno Org. Biomol. Chem. 2012 10 2870
2. Hydrosilylation of cinchonidine and 9-O-TMS-cinchonidine with triethoxysilane: application of 11-(triethoxysilyl)-10,11-dihydrocinchonidine as a chiral modifier in the enantioselective hydrogenation of 1-phenylpropane-1,2-dione
Anna Lindholm,P?ivi M?ki-Arvela,Esa Toukoniitty,Tapani A. Pakkanen,Janne T. Hirvi,Tapio Salmi,Dmitry Yu. Murzin,Rainer Sj?holm,Reko Leino J. Chem. Soc. Perkin Trans. 1 2002 2605
3. Diastereo- and enantioselective synthesis of α,β-epoxyketones using aqueous NaOCl in conjunction with dihydrocinchonidine derived phase-transfer catalysis at room temperature. Scope and limitations
Barry Lygo,Stuart D. Gardiner,Michael C. McLeod,Daniel C. M. To Org. Biomol. Chem. 2007 5 2283
4. XPS and LEED studies of 10,11-dihydrocinchonidine adsorption at Pt(111). Implications for the role of cinchona alkaloids in enantioselective hydrogenation
A. F. Carley,M. K. Rajumon,M. W. Roberts,P. B. Wells J. Chem. Soc. Faraday Trans. 1995 91 2167
5. Cinchona-based phase-transfer catalysts for asymmetric synthesis
Sang-sup Jew,Hyeung-geun Park Chem. Commun. 2009 7090
6. Emerging strategies in sustainable fine-chemical synthesis: asymmetric catalysis by metal nanoparticles
Pierluigi Barbaro,Vladimiro Dal Santo,Francesca Liguori Dalton Trans. 2010 39 8391
7. Kinetics and catalyst deactivation in the enantioselective hydrogenation of ethyl benzoylformate over Pt/Al2O3
Gerson Martin,P?ivi M?ki-Arvela,Dmitry Yu. Murzin,Tapio Salmi Catal. Sci. Technol. 2014 4 170
8. Pt nanoparticles stabilized by thermosensitive polymer as effective and recyclable catalysts for the asymmetric hydrogenation of ethyl pyruvate
Wenjun Yu,Lan-Lan Lou,Kai Yu,Shanshan Li,Yang Shi,Shuangxi Liu RSC Adv. 2016 6 52500
9. Enantioselective desymmetrization of prochiral 1,3-dinitropropanes via organocatalytic allylic alkylation
Soumya Jyoti Singha Roy,Santanu Mukherjee Chem. Commun. 2014 50 121
10. Enantioselective desymmetrization of prochiral 1,3-dinitropropanes via organocatalytic allylic alkylation
Soumya Jyoti Singha Roy,Santanu Mukherjee Chem. Commun. 2014 50 121

氢化辛可宁丁 | 485-64-3

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