4-(4-甲氧基苯基)噻唑-2-胺

• 常用名: 4-(4-甲氧基苯基)噻唑-2-胺
• 英文名: 4-(4-Methoxyphenyl)thiazol-2-amine
• CAS号: 2104-04-3
• 分子量: 206.26400
• 密度: 1.259 g/cm3
• 沸点: 396.7ºC at 760 mmHg
• 分子式: C₁₀H₁₀N₂OS
• 熔点: 204-208ºC
• 闪点: 193.7ºC

4-(4-甲氧基苯基)噻唑-2-胺名称

• 中文名: 4-(4-甲氧基苯基)-1,3-噻唑-2-胺
• 英文名: 4-(4-Methoxyphenyl)-1,3-thiazol-2-amine

4-(4-甲氧基苯基)噻唑-2-胺物理化学性质

• 密度: 1.259 g/cm3
• 沸点: 396.7ºC at 760 mmHg
• 熔点: 204-208ºC
• 分子式: C₁₀H₁₀N₂OS
• 分子量: 206.26400
• 闪点: 193.7ºC
• 精确质量: 206.05100
• PSA: 76.38000
• LogP: 2.98210
• InChIKey: YPVVEXKDPBRGIK-UHFFFAOYSA-N
• SMILES: COc1ccc(-c2csc(N)n2)cc1
• 蒸汽压: 1.67E-06mmHg at 25°C
• 折射率: 1.629
• 储存条件: 2-8℃，避光，干燥，密封

4-(4-甲氧基苯基)噻唑-2-胺MSDS

4-(4-甲氧基苯基)噻唑-2-胺MSDS英文版

4-(4-甲氧基苯基)噻唑-2-胺毒性和生态

4-(4-甲氧基苯基)噻唑-2-胺安全信息

• 危害码 (欧洲): Xi: Irritant;
• 风险声明 (欧洲): 22
• 海关编码: 2934100090

4-(4-甲氧基苯基)噻唑-2-胺海关

• 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%

4-(4-甲氧基苯基)噻唑-2-胺靶点实验

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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

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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：Binding affinity to Plasmodium falciparum AMA1 at 200 uM by surface plasmon resonance... 来源：ChEMBL 靶标：Apical membrane antigen 1 External Id：CHEMBL3414329

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：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：Inhibition of amyloid beta (1 to 42) self-aggregation at 20 uM after 24 hrs by thiofl... 来源：ChEMBL 靶标：N/A External Id：CHEMBL2162684

实验名称：High throughput fluorescence intensity-based biochemical assay to screen for small mo... 来源：University of Pittsburgh Molecular Library Screening Center 靶标：furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens] External Id：MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.

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

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4-(4-甲氧基苯基)噻唑-2-胺英文别名

• MFCD00170663