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5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide

更新时间:2025-10-06 19:39:52

5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide结构式
5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide结构式
委托求购
常用名 5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide 英文名 5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide
CAS号 52868-69-6 分子量 189.25900
密度 1.52g/cm3 沸点 422.3ºC at 760 mmHg
分子式 C5H7N3OS2 熔点 N/A
MSDS N/A 闪点 209.2ºC

 名称

英文名 5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide
英文别名 更多

 物理化学性质

密度 1.52g/cm3
沸点 422.3ºC at 760 mmHg
分子式 C5H7N3OS2
分子量 189.25900
闪点 209.2ºC
精确质量 189.00300
PSA 135.54000
LogP 1.82760
InChIKey ZGYKQSVGGNYQKY-UHFFFAOYSA-N
SMILES CSc1nc(C(N)=O)c(N)s1
折射率 1.69

 合成线路

~96%

5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide结构式

5-amino-2-methy...

52868-69-6

文献:Wang, Jin; Guo, Jianyu; Tang, Yihong; Zhang, Suxia; Tao, Jianwei; Lu, Yan Heterocyclic Communications, 2014 , vol. 20, # 3 p. 175 - 176

 靶点实验

查看更多实验

实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:Modulation of human adenosine A1 receptor expressed in CHO-K1 cells assessed as stabi...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL1032276
实验名称:Inhibitors of CDC25B-CDK2/CyclinA interaction
来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
实验名称:ASTRAZENECA: Octan-1-ol/water (pH7.4) distribution coefficent measured by a shake fl...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL3301363
实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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
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 英文别名

5-amino-2-methylthiothiazole-4-carboxamide
5-amino-2-methylsulfanylthiazole-4-carboxamide
5-Amino-2-methylmercapto-thiazol-4-carbonsaeure-amid
5-amino-2-methylsulfanyl-thiazole-4-carboxylic acid amide
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