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6-phenyl-2-sulfanylidene-1,3-diazinan-4-one

更新时间:2025-09-27 18:37:05

6-phenyl-2-sulfanylidene-1,3-diazinan-4-one结构式
6-phenyl-2-sulfanylidene-1,3-diazinan-4-one结构式
委托求购
常用名 6-phenyl-2-sulfanylidene-1,3-diazinan-4-one 英文名 6-phenyl-2-sulfanylidene-1,3-diazinan-4-one
CAS号 6300-96-5 分子量 206.26400
密度 1.32g/cm3 沸点 N/A
分子式 C10H10N2OS 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 6-phenyl-2-sulfanylidene-1,3-diazinan-4-one
英文别名 更多

 物理化学性质

密度 1.32g/cm3
分子式 C10H10N2OS
分子量 206.26400
精确质量 206.05100
PSA 73.22000
LogP 1.77970
InChIKey JIBRFUJNQRGYJA-UHFFFAOYSA-N
SMILES O=C1CC(c2ccccc2)NC(=S)N1
折射率 1.664

 合成线路

~33%

6-phenyl-2-sulfanylidene-1,3-diazinan-4-one结构式

6-phenyl-2-sulf...

6300-96-5

文献:Svetlik, Jan; Veizerova, Lucia Helvetica Chimica Acta, 2011 , vol. 94, # 2 p. 199 - 205

~%

6-phenyl-2-sulfanylidene-1,3-diazinan-4-one结构式

6-phenyl-2-sulf...

6300-96-5

文献:Erlenmeyer; Heitz Helvetica Chimica Acta, 1942 , vol. 25, p. 832,834

~%

6-phenyl-2-sulfanylidene-1,3-diazinan-4-one结构式

6-phenyl-2-sulf...

6300-96-5

文献:Posner Chemische Berichte, 1905 , vol. 38, p. 2324,2719

 靶点实验

查看更多实验

实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_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 polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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 英文别名

HMS1688M03
2-Mercapto-6-phenyl-5,6-dihydro-3H-pyrimidin-4-one
4-Phenyl-dihydro-thiouracil
6-phenyl-2-thioxo-tetrahydro-pyrimidin-4-one
6-Phenyl-2-thioxo-tetrahydro-pyrimidin-4-on
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