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4,6-双(甲基硫代)嘧啶

更新时间:2025-08-25 18:20:18

4,6-双(甲基硫代)嘧啶结构式
4,6-双(甲基硫代)嘧啶结构式
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常用名 4,6-双(甲基硫代)嘧啶 英文名 Pyrimidine,4,6-bis(methylthio)
CAS号 1450-90-4 分子量 172.27100
密度 1.26g/cm3 沸点 294.5ºC at 760mmHg
分子式 C6H8N2S2 熔点 N/A
MSDS N/A 闪点 131.9ºC

 4,6-双(甲基硫代)嘧啶名称

中文名 4,6-双(甲基硫代)嘧啶
英文名 4,6-bis(methylsulfanyl)pyrimidine
英文别名 更多

 4,6-双(甲基硫代)嘧啶物理化学性质

密度 1.26g/cm3
沸点 294.5ºC at 760mmHg
分子式 C6H8N2S2
分子量 172.27100
闪点 131.9ºC
精确质量 172.01300
PSA 76.38000
LogP 1.92040
InChIKey PDEXXTHEMNGLQV-UHFFFAOYSA-N
SMILES CSc1cc(SC)ncn1
蒸汽压 0.00284mmHg at 25°C
折射率 1.615

 4,6-双(甲基硫代)嘧啶合成线路

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4,6-双(甲基硫代)嘧啶结构式

4,6-双(甲基硫代)嘧啶

1450-90-4

文献:IRM LLC; NOVARTIS AG Patent: WO2008/42639 A1, 2008 ; Location in patent: Page/Page column 69 ; WO 2008/042639 A1

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4,6-双(甲基硫代)嘧啶结构式

4,6-双(甲基硫代)嘧啶

1450-90-4

文献:Porter, John R; Archibald, Sarah C; Brown, Julien A; Childs, Kirstie; Critchley, David; Head, John C; Hutchinson, Brian; Parton, Ted A H; Robinson, Martyn K; Shock, Anthony; Warrellow, Graham J; Zomaya, Alex Bioorganic and medicinal chemistry letters, 2002 , vol. 12, # 12 p. 1595 - 1598

 4,6-双(甲基硫代)嘧啶上下游产品

4,6-双(甲基硫代)嘧啶上游产品  2

4,6-双(甲基硫代)嘧啶下游产品  0

 4,6-双(甲基硫代)嘧啶靶点实验

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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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: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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
实验名称:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
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 4,6-双(甲基硫代)嘧啶英文别名

4,6-Bis-methylmercapto-pyrimidin
4,6-bis-methylsulfanyl-pyrimidine
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