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6-benzoyl-2,5-diphenyl-pyridazin-3-one

更新时间:2025-09-25 11:35:33

6-benzoyl-2,5-diphenyl-pyridazin-3-one结构式
6-benzoyl-2,5-diphenyl-pyridazin-3-one结构式
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常用名 6-benzoyl-2,5-diphenyl-pyridazin-3-one 英文名 6-benzoyl-2,5-diphenyl-pyridazin-3-one
CAS号 75872-31-0 分子量 352.38500
密度 1.17g/cm3 沸点 533.1ºC at 760 mmHg
分子式 C23H16N2O2 熔点 N/A
MSDS N/A 闪点 276.2ºC

 6-benzoyl-2,5-diphenyl-pyridazin-3-one名称

英文名 6-benzoyl-2,5-diphenylpyridazin-3-one
英文别名 更多

 6-benzoyl-2,5-diphenyl-pyridazin-3-one物理化学性质

密度 1.17g/cm3
沸点 533.1ºC at 760 mmHg
分子式 C23H16N2O2
分子量 352.38500
闪点 276.2ºC
精确质量 352.12100
PSA 51.96000
LogP 4.13050
InChIKey SRDKDQFRXJKIOF-UHFFFAOYSA-N
SMILES O=C(c1ccccc1)c1nn(-c2ccccc2)c(=O)cc1-c1ccccc1
折射率 1.635

 6-benzoyl-2,5-diphenyl-pyridazin-3-one合成线路

~91%

6-benzoyl-2,5-diphenyl-pyridazin-3-one结构式

6-benzoyl-2,5-d...

75872-31-0

文献:Bestmann, Hans Juergen; Schmid, Guenter; Sandmeier, Dieter Tetrahedron Letters, 1980 , vol. 21, p. 2939 - 2942

~%

6-benzoyl-2,5-diphenyl-pyridazin-3-one结构式

6-benzoyl-2,5-d...

75872-31-0

文献:Patel; Vyas; Pandey; Tavares; Fernandes Synthetic Communications, 1991 , vol. 21, # 8-9 p. 1021 - 1026

~%

6-benzoyl-2,5-diphenyl-pyridazin-3-one结构式

6-benzoyl-2,5-d...

75872-31-0

文献:Patel; Vyas; Pandey; Tavares; Fernandes Synthetic Communications, 1991 , vol. 21, # 18-19 p. 1935 - 1940

 6-benzoyl-2,5-diphenyl-pyridazin-3-one上下游产品

6-benzoyl-2,5-diphenyl-pyridazin-3-one上游产品  4

6-benzoyl-2,5-diphenyl-pyridazin-3-one下游产品  0

 6-benzoyl-2,5-diphenyl-pyridazin-3-one靶点实验

查看更多实验

实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Luciferase Reporter Cell Based HTS to identify inhibitors of N-linked Glycosylation M...
来源:Broad Institute
靶标:N/A
External Id:2146-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Confirmatory qHTS for agonist of cAMP-regulated guanine nucleotide exchange factor 3 ...
来源:NCGC
External Id:epac1-activator-f1f2f3f4
实验名称:Confirmatory qHTS for antagonist of cAMP-regulated guanine nucleotide exchange factor...
来源:NCGC
External Id:epac1-inhibitor-f1f2f3f4
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 6-benzoyl-2,5-diphenyl-pyridazin-3-one英文别名

6-Benzoyl-2,5-diphenyl-3(2H)-pyridazinon
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