N-(3-chlorophenyl)-4,5-dihydro-1,3-thiazol-2-amine

• 常用名: N-(3-chlorophenyl)-4,5-dihydro-1,3-thiazol-2-amine
• 英文名: N-(3-chlorophenyl)-4,5-dihydro-1,3-thiazol-2-amine
• CAS号: 83890-29-3
• 分子量: 212.69900
• 密度: 1.38g/cm3
• 沸点: 328.7ºC at 760 mmHg
• 分子式: C₉H₉ClN₂S
• 熔点: N/A
• 闪点: 152.6ºC

名称

• 英文名: N-(3-chlorophenyl)-4,5-dihydro-1,3-thiazol-2-amine

物理化学性质

• 密度: 1.38g/cm3
• 沸点: 328.7ºC at 760 mmHg
• 分子式: C₉H₉ClN₂S
• 分子量: 212.69900
• 闪点: 152.6ºC
• 精确质量: 212.01700
• PSA: 49.69000
• LogP: 2.36330
• InChIKey: GBQKVBOQHMFWHS-UHFFFAOYSA-N
• SMILES: Clc1cccc(NC2=NCCS2)c1
• 折射率: 1.67

安全信息

• 海关编码: 2934100090

海关

• 海关编码: 2934100090
• 中文概述: 2934100090. 结构上含有一个非稠合噻唑环的化合物(不论是否氢化). 增值税率:17.0%. 退税率:9.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
• 申报要素: 品名, 成分含量, 用途
• Summary: 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

靶点实验

查看更多实验

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：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

实验名称：Fluorescence polarization-based biochemical high throughput primary assay to identify... 来源：The Scripps Research Institute Molecular Screening Center 靶标：abhydrolase domain-containing protein 4 isoform 1 [Mus musculus] External Id：ABHD4_INH_FP_1536_1X%INH PRUN

实验名称：High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati... 来源：Southern Research Institute 靶标：HIV-1 Vif External Id：HIV1-VIF_MS

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英文别名

• (3-chloro-phenyl)-(4,5-dihydro-thiazol-2-yl)-amine
• (3-Chlor-phenyl)-(4,5-dihydro-thiazol-2-yl)-amin