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N-(萘-2-基)-3-氧代丁酰胺

更新时间:2025-08-25 19:23:51

N-(萘-2-基)-3-氧代丁酰胺结构式
N-(萘-2-基)-3-氧代丁酰胺结构式
品牌特惠专场
常用名 N-(萘-2-基)-3-氧代丁酰胺 英文名 N-(2-naphthyl)-3-oxobutanamide
CAS号 42414-19-7 分子量 227.25900
密度 1.216g/cm3 沸点 471.5ºC at 760 mmHg
分子式 C14H13NO2 熔点 N/A
MSDS N/A 闪点 198.8ºC

 N-(萘-2-基)-3-氧代丁酰胺名称

中文名 N-(萘-2-基)-3-氧代丁酰胺
英文名 N-naphthalen-2-yl-3-oxobutanamide

 N-(萘-2-基)-3-氧代丁酰胺物理化学性质

密度 1.216g/cm3
沸点 471.5ºC at 760 mmHg
分子式 C14H13NO2
分子量 227.25900
闪点 198.8ºC
精确质量 227.09500
PSA 46.17000
LogP 2.83040
InChIKey SJZXYYGWOBQVKI-UHFFFAOYSA-N
SMILES CC(=O)CC(=O)Nc1ccc2ccccc2c1
折射率 1.644

 N-(萘-2-基)-3-氧代丁酰胺合成线路

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N-(萘-2-基)-3-氧代丁酰胺结构式

N-(萘-2-基)-3-氧代丁酰胺

42414-19-7

文献:Carbide and Carbon Chem.Corp. Patent: US2152787 , 1937 ; Full Text Show Details Carbide and Carbon Chem.Corp. Patent: US2152786 , 1936 ;

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N-(萘-2-基)-3-氧代丁酰胺结构式

N-(萘-2-基)-3-氧代丁酰胺

42414-19-7

文献:Dilthey; Kaiser Justus Liebigs Annalen der Chemie, 1949 , vol. 563, p. 11,14

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N-(萘-2-基)-3-氧代丁酰胺结构式

N-(萘-2-基)-3-氧代丁酰胺

42414-19-7

文献:Albert et al. Journal of the Chemical Society, 1948 , p. 1284,1290

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N-(萘-2-基)-3-氧代丁酰胺结构式

N-(萘-2-基)-3-氧代丁酰胺

42414-19-7

文献:Knorr Chemische Berichte, 1884 , vol. 17, p. 542 Justus Liebigs Annalen der Chemie, 1888 , vol. 245, p. 368 Full Text Show Details Conrad; Limpach Chemische Berichte, 1888 , vol. 21, p. 531

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N-(萘-2-基)-3-氧代丁酰胺结构式

N-(萘-2-基)-3-氧代丁酰胺

42414-19-7

文献:Knorr Chemische Berichte, 1884 , vol. 17, p. 542 Justus Liebigs Annalen der Chemie, 1888 , vol. 245, p. 368

 N-(萘-2-基)-3-氧代丁酰胺靶点实验

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External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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来源:Burnham Center for Chemical Genomics
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External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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External Id:CHEMBL4296186
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External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
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External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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