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3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮

更新时间:2025-08-27 23:15:22

3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮结构式
3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮结构式
品牌特惠专场
常用名 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮 英文名 3-(4-Fluorophenyl)-2-thioxo-1,3-thiazolidin-4-one
CAS号 387-27-9 分子量 227.27800
密度 1.53g/cm3 沸点 339ºC at 760mmHg
分子式 C9H6FNOS2 熔点 N/A
MSDS N/A 闪点 158.9ºC

 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮名称

中文名 3-(4-氟苯基)-2-硫基氧代-1,3-噻唑烷-4-酮
英文名 3-(4-fluorophenyl)-2-sulfanylidene-1,3-thiazolidin-4-one
英文别名 更多

 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮物理化学性质

密度 1.53g/cm3
沸点 339ºC at 760mmHg
分子式 C9H6FNOS2
分子量 227.27800
闪点 158.9ºC
精确质量 226.98700
PSA 77.70000
LogP 2.25540
InChIKey KQOPBWMREOTAOQ-UHFFFAOYSA-N
SMILES O=C1CSC(=S)N1c1ccc(F)cc1
折射率 1.707
储存条件 室温

 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮安全信息

危害码 (欧洲) Xi: Irritant;

 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮合成线路

~74%

3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮结构式

3-(4-氟苯基)-2-硫亚基...

387-27-9

文献:MICROBIOTIX, INC. Patent: WO2009/142720 A1, 2009 ; Location in patent: Page/Page column 31-32 ;

~39%

3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮结构式

3-(4-氟苯基)-2-硫亚基...

387-27-9

文献:Nitsche, Christoph; Schreier, Verena N.; Behnam, Mira A. M.; Kumar, Anil; Bartenschlager, Ralf; Klein, Christian D. Journal of Medicinal Chemistry, 2013 , vol. 56, # 21 p. 8389 - 8403

 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮上下游产品

3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮上游产品  4

3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮下游产品  0

 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Fluorescence-based counterscreen for orexin 1 receptor (OX1R) antagonists: cell-based...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:CHOK1_ANT_FLUO8_1536_1X%INH CSRUN
实验名称:qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2
来源:NCGC
靶标:eyes absent homolog 2 isoform a [Homo sapiens]
External Id:EYA2477
实验名称:Absorbance-based primary biochemical high throughput screening assay to identify acti...
来源:The Scripps Research Institute Molecular Screening Center
靶标:caspase-3 preproprotein [Homo sapiens]
External Id:PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:Primary cell-based high-throughput screening for identification of compounds that all...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_AlloAgonist_Primary
实验名称:uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent a...
来源:Burnham Center for Chemical Genomics
靶标:TPA: Essential component of the Translocase of the Inner Mitochondrial membrane (TIM23 complex); involved in protein import into mitochondrial matrix and inner membrane; with Tim17p, contributes to architecture and function of the import channel [Saccharomyces cerevisiae S288c]
External Id:SBCCG-A419-tim23-1-Primary-Antagonist-Assay
实验名称:Primary cell-based high-throughput screening for identification of compounds that ant...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_Antagonist_Primary
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
实验名称:Counterscreen for procaspase-3 activators: absorbance-based primary biochemical high ...
来源:The Scripps Research Institute Molecular Screening Center
靶标:caspase 7, apoptosis-related cysteine peptidase [Homo sapiens]
External Id:PROCASPASE7_ACT_EPIABS_1536_1X%ACT CSRUN
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 3-(4-氟苯基)-2-硫亚基-1,3-噻唑烷-4-酮英文别名

4-fluorophenyl rhodanine
3-(4-Fluorophenyl)rhodanine
3-(4-Fluor-phenyl)-2-thioxo-thiazolidin-4-on
fluorophenylthioxothiazolanone
3-(4-fluorophenyl)-2-thioxothiazolidin-4-one
3-(4-fluorophenyl)-2-thioxo-1,3-thiazolidin-4-one
3-(4'-Fluorphenyl)-rhodanin
3-(4-fluorophenyl)-2-thioxo-1,3-thiazolan-4-one
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