前往化源商城

2H-1,4-Benzothiazine-2-aceticacid, 3,4-dihydro-3-oxo-, 2-(4-fluorophenyl)hydrazide

更新时间:2025-09-12 18:08:51

2H-1,4-Benzothiazine-2-aceticacid, 3,4-dihydro-3-oxo-, 2-(4-fluorophenyl)hydrazide结构式
2H-1,4-Benzothiazine-2-aceticacid, 3,4-dihydro-3-oxo-, 2-(4-fluorophenyl)hydrazide结构式
委托求购
常用名 2H-1,4-Benzothiazine-2-aceticacid, 3,4-dihydro-3-oxo-, 2-(4-fluorophenyl)hydrazide 英文名 2H-1,4-Benzothiazine-2-aceticacid, 3,4-dihydro-3-oxo-, 2-(4-fluorophenyl)hydrazide
CAS号 2263-58-3 分子量 331.36500
密度 1.381g/cm3 沸点 514.6ºC at 760mmHg
分子式 C16H14FN3O2S 熔点 N/A
MSDS N/A 闪点 265ºC

 名称

英文名 (3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-essigsaeure-[N'-(4-fluor-phenyl)-hydrazid]
英文别名 更多

 物理化学性质

密度 1.381g/cm3
沸点 514.6ºC at 760mmHg
分子式 C16H14FN3O2S
分子量 331.36500
闪点 265ºC
精确质量 331.07900
PSA 95.53000
LogP 3.37380
InChIKey HWUGMQFMAKVBQO-UHFFFAOYSA-N
SMILES O=C(CC1Sc2ccccc2NC1=O)NNc1ccc(F)cc1
蒸汽压 1.06E-10mmHg at 25°C
折射率 1.65

 上下游产品

上游产品  1

下游产品  0

 靶点实验

查看更多实验

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
共96条,当前第1页,共10页
1
2
3
4
5

 英文别名

(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-acetic acid-(3-chloro-anilide)
N-(2-Chlorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine-2-acetamide
(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-acetic acid-[N'-(4-fluoro-phenyl)-hydrazide]
(3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-essigsaeure-(3-chlor-anilid)
2H-1,4-Benzothiazine-2-acetamide,3,4-dihydro-N-(2-chlorophenyl)-3-oxo
N-(3-chlorophenyl)-2-(3-oxo-1,4-benzothiazin-2-yl) acetamide
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。