地诺帕明 | 71771-90-9
地诺帕明
(R)-(-)-Denopamine
71771-90-9
C18H23NO4
317.379
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:地诺帕明结构式
名称和标识符
InChIKey |
VHSBBVZJABQOSG-INIZCTEOSA-N |
Inchi |
InChI=1S/C18H23NO4/c1-22-17-8-3-13(11-18(17)23-2)9-10-19-12-16(21)14-4-6-15(20)7-5-14/h3-8,11,16,19-21H,9-10,12H2,1-2H3/t16-/m0/s1 |
SMILES |
O(C)C1=CC(CCNC[C@@H](C2C=CC(=CC=2)O)O)=CC=C1OC |
别名信息
- 中文别名 -
- 地诺帕明
- 待罗把胺
- 甲氧丁巴胺
- cis-15-二十四烯酸甲酯
- -Α-[[[2-(3,4-二甲氧基苯基)乙基]氨基]甲基]-4-羟基苯甲醇
- 英文别名 -
- Denopamine
- R(-)-DENOPAMINE
- (-)-ALPHA-(3,4-DIMETHOXYPHENETHYLAMINOMETHYL)-4-HYDROXYBENZYLALCOHOL
- (-)-(r)-1-(p-hydroxyphenyl)-2-((3,4-dimethoxyphenethyl)amino)ethanol
- alpha-(((2-(3,4-dimethoxyphenyl)ethyl)amino)methyl)-4-hydroxy-benzenemethano
- (R)-(-)-Denopamine
- (-)-(R)-1-(p-hydroxyphenyl)-2-<(3,4-dimehoxyphenethyl)amino>ethanol
- (-)-(R)-1-(p-hydroxyphenyl)-2-<(3,4-dimethoxyphenethyl)amino>ethanol
- (-)-Denopamine
- (R)-1-(4-Hydroxyphenyl)-2-(3,4-dimethoxyphenethylamino)ethanol
- (R)-4-{2-[2-(3,4-dimethoxy-phenyl)-ethylamino]-1-hydroxy-ethyl}-phenol
- Carguto
- kalgut
- TA 064
- HX-215
- (R)-(-)-Denopamine
物化性质
实验特性
LogP |
2.66600 |
PSA |
70.95000 |
折射率 |
1.5740 (estimate) |
沸点 |
456.67°C (rough estimate) |
熔点 |
135°C |
溶解度 |
DMSO: 26 mg/mL, soluble |
密度 |
1.1949 (rough estimate) |
计算特性
相关文献
-
1.
A facile approach towards enantiomerically pure masked β-amino alcohols
Pankaj Gupta,Bhahwal Ali Shah,Rajinder Parshad,Ghulam Nabi Qazi,Subhash Chandra Taneja Green Chem. 2007 9 1120
-
2.
Daucus carota L. mediated bioreduction of prochiral ketones
Nicolas Blanchard,Pierre van de Weghe Org. Biomol. Chem. 2006 4 2348
-
3.
Daucus carota L. mediated bioreduction of prochiral ketones
Nicolas Blanchard,Pierre van de Weghe Org. Biomol. Chem. 2006 4 2348
-
4.
Production of chiral compounds using immobilized cells as a source of biocatalysts
Camila M. Kisukuri,Leandro H. Andrade Org. Biomol. Chem. 2015 13 10086
-
5.
Biocatalytic approaches for enantio and diastereoselective synthesis of chiral β-nitroalcohols
D. H. Sreenivasa Rao,Ayon Chatterjee,Santosh Kumar Padhi Org. Biomol. Chem. 2021 19 322
-
6.
An overview of Zn-catalyzed enantioselective aldol type C–C bond formation
Amrutha P. Thankachan,S. Asha,K. S. Sindhu,Gopinathan Anilkumar RSC Adv. 2015 5 62179
-
7.
Efficient access to chiral 1,2-amino alcohols via Ir/f-amphox-catalyzed asymmetric hydrogenation of α-amino ketones
Yang Hu,Weilong Wu,Xiu-Qin Dong,Xumu Zhang Org. Chem. Front. 2017 4 1499
-
8.
Protective effects of clovamide against H2O2-induced stress in rat cardiomyoblasts H9c2 cell line
Andrea Zamperone,Stefano Pietronave,Donato Colangelo,Silvia Antonini,Monica Locatelli,Fabiano Travaglia,Jean Daniel Co?sson,Marco Arlorio,Maria Prat Food Funct. 2014 5 2542
-
9.
Biocatalytic deuterium- and hydrogen-transfer using over-expressed ADH-‘A’: enhanced stereoselectivity and 2H-labeled chiral alcohols
Klaus Edegger,Christian C. Gruber,Tina M. Poessl,Sabine R. Wallner,Iván Lavandera,Kurt Faber,Frank Niehaus,Juergen Eck,Reinhold Oehrlein,Andreas Hafner,Wolfgang Kroutil Chem. Commun. 2006 2402
-
10.
Carrier enabled catalytic reaction cascades
Lars Veum,Ulf Hanefeld Chem. Commun. 2006 825
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