2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide

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Company Name: Shanghai Raise Chemical Technology Co.,Ltd  
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Email: rs@raise-chem.com
Company Name: Amatek Scientific Co. Ltd.  
Tel: 0512-56316828 400-867-5858;400-867-5858
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Company Name: Nextpeptide Inc  
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Company Name: Shanghai Dongyang Biotechnology Co., Ltd.  
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2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide manufacturers

2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide Basic information
Product Name:2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide
Synonyms:2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide;Benzamide, 2-(2-aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)-;HJC0152 free base
CAS:1420290-88-5
MF:C15H13Cl2N3O4
MW:370.19
EINECS:
Product Categories:
Mol File:1420290-88-5.mol
2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide Structure
2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide Chemical Properties
Boiling point 486.2±45.0 °C(Predicted)
density 1.491±0.06 g/cm3(Predicted)
storage temp. Store at Room Tem.
pka10.93±0.70(Predicted)
Safety Information
MSDS Information
2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide Usage And Synthesis
UsesHJC0152 (free base) is an orally active and potent inhibitor of STAT3. HJC0152 (free base) inhibits cell cycle progression and induces apoptosis. HJC0152 (free base) significantly suppresses MDA-MB-231 xenograft tumor growth in mice[1].
References[1] Chen H, et al. Discovery of O-Alkylamino Tethered Niclosamide Derivatives as Potent and Orally Bioavailable Anticancer Agents. ACS Med Chem Lett. 2013 Feb 14;4(2):180-185. DOI:10.1021/ml3003082
2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide Preparation Products And Raw materials
Tag:2-(2-Aminoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide(1420290-88-5) Related Product Information
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