1256387-74-2|(1R,3S,4S)-3-(6-Bromo-1H-benzimidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylic acid 1,1-dimethylethyl ester

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(1R,3S,4S)-3-(6-Bromo-1H-benzimidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylic acid 1,1-dimethylethyl ester | CAS:1256387-74-2

(1R,3S,4S)-3-(6-Bromo-1H-benzimidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylic acid 1,1-dimethylethyl ester

Name：(1R,3S,4S)-3-(6-Bromo-1H-benzimidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylic acid 1,1-dimethylethyl ester
CAS：1256387-74-2
Synonyms：
Molecular Formula：C₁₈H₂₂BrN₃O₂
Molecular Weight：392.29
EINESC：

Description

Properties

Density	1.455±0.06 g/cm3 (20 º

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Source	SDS/MSDS Samples
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Synthetic Route

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Ledipasvir	1256388-51-8	View

Articles

Peer-Reviewed Papers

Silica-supported quinolinium tribromide: a recoverable solid brominating reagent for regioselective monobromination of aromatic amines.Li Z, et al. Journal of the Brazilian Chemical Society, 21(3), 496-501 (2010) Efficient synthesis of 2-amino-6-arylbenzothiazoles via Pd (0) Suzuki cross coupling reactions: potent urease enzyme inhibition and nitric oxide scavenging activities of the products.Gull Y, et al. Molecules (Basel), 18(8), 8845-8857 (2013) Synthesis, cytostatic, and antitumor properties of new Rh (I) thiazole complexes. Craciunescu, D. G., et al. Biological trace element research, 8(4), 251-261 (1985) Prokaryotic NavMs channel as a structural and functional model for eukaryotic sodium channel antagonism.Claire Bagnéris et al.Proceedings of the National Academy of Sciences of the United States of America, 111(23), 8428-8433 (2014-05-23)

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