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5-环己基氨基-[1,3,4]噻二唑-2-硫醇

更新时间:2025-08-27 10:40:19

5-环己基氨基-[1,3,4]噻二唑-2-硫醇结构式
5-环己基氨基-[1,3,4]噻二唑-2-硫醇结构式
品牌特惠专场
常用名 5-环己基氨基-[1,3,4]噻二唑-2-硫醇 英文名 5-(cyclohexylamino)-3H-1,3,4-thiadiazole-2-thione
CAS号 68161-70-6 分子量 215.33900
密度 1.52g/cm3 沸点 312.4ºC at 760 mmHg
分子式 C8H13N3S2 熔点 N/A
MSDS N/A 闪点 142.7ºC

 5-环己基氨基-[1,3,4]噻二唑-2-硫醇名称

中文名 5-环己基氨基-[1,3,4]噻二唑-2-硫醇
英文名 5-(cyclohexylamino)-3H-1,3,4-thiadiazole-2-thione
英文别名 更多

 5-环己基氨基-[1,3,4]噻二唑-2-硫醇物理化学性质

密度 1.52g/cm3
沸点 312.4ºC at 760 mmHg
分子式 C8H13N3S2
分子量 215.33900
闪点 142.7ºC
精确质量 215.05500
PSA 101.04000
LogP 3.01830
InChIKey JOPULZODGGQCOM-UHFFFAOYSA-N
SMILES S=c1[nH]nc(NC2CCCCC2)s1
折射率 1.765

 5-环己基氨基-[1,3,4]噻二唑-2-硫醇MSDS

 5-环己基氨基-[1,3,4]噻二唑-2-硫醇合成线路

~%

5-环己基氨基-[1,3,4]噻二唑-2-硫醇结构式

5-环己基氨基-[1,3,4]...

68161-70-6

文献:Wahab Bollettino Chimico Farmaceutico, 1979 , vol. 118, # 7 p. 391 - 396

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 5-环己基氨基-[1,3,4]噻二唑-2-硫醇靶点实验

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实验名称:C. difficile toxins: Counterscreen in absence of substrate UDPG Measured in Biochemic...
来源:Broad Institute
靶标:N/A
External Id:7074-02_Inhibitor_Dose_CherryPick_Activity
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:C. difficile toxins: HTS for inhibitors of TcdB glycohydrolase activity Measured in B...
来源:Broad Institute
靶标:Toxin B [Clostridium difficile 630]
External Id:7074-01_Inhibitor_Dose_CherryPick_Activity
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
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 5-环己基氨基-[1,3,4]噻二唑-2-硫醇英文别名

5-cyclohexylamino-3H-[1,3,4]thiadiazole-2-thione
5-(cyclohexylamino)-1,3,4-thiadiazole-2-thiol
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