2-(4-羟基苯基)噻唑结构式
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常用名 | 2-(4-羟基苯基)噻唑 | 英文名 | 4-(2-Thiazolyl)phenol |
|---|---|---|---|---|
| CAS号 | 81015-49-8 | 分子量 | 177.22300 | |
| 密度 | 1.363 g/cm3 | 沸点 | 282.7ºC at 760 mmHg | |
| 分子式 | C9H7NOS | 熔点 | 162-165°C | |
| MSDS | N/A | 闪点 | 124.8ºC |
| 中文名 | 2-(4-羟基苯基)噻唑 |
|---|---|
| 英文名 | 4-(2-Thiazolyl)phenol |
| 中文别名 | 4-(2-噻唑基)苯酚 |
| 英文别名 | 更多 |
| 密度 | 1.363 g/cm3 |
|---|---|
| 沸点 | 282.7ºC at 760 mmHg |
| 熔点 | 162-165°C |
| 分子式 | C9H7NOS |
| 分子量 | 177.22300 |
| 闪点 | 124.8ºC |
| 精确质量 | 177.02500 |
| PSA | 61.36000 |
| LogP | 2.51570 |
| InChIKey | PXNRJZLHXKIISI-UHFFFAOYSA-N |
| SMILES | Oc1ccc(-c2nccs2)cc1 |
| 折射率 | 1.644 |
| 储存条件 | 室温,干燥 |
| 危害码 (欧洲) | Xi |
|---|---|
| 海关编码 | 2934100090 |
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~93%
2-(4-羟基苯基)噻唑 81015-49-8 |
| 文献:Sun, Min; Wu, Xiaoqing; Chen, Junqing; Cai, Jin; Cao, Meng; Ji, Min European Journal of Medicinal Chemistry, 2010 , vol. 45, # 6 p. 2299 - 2306 |
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~60%
2-(4-羟基苯基)噻唑 81015-49-8 |
| 文献:SUNSHINE LAKE PHARMA CO., LTD.; ZHANG, Yingjun; ZHANG, Jiancun; WANG, Xiaojun; LIN, Runfeng; CAO, Shengtian; WANG, Zhaohe; LI, Jing Patent: WO2014/12360 A1, 2014 ; Location in patent: Paragraph 00266 ; |
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~28%
2-(4-羟基苯基)噻唑 81015-49-8 |
| 文献:Jensen; Skjaerbaek; Vedso Synthesis, 2001 , # 1 p. 128 - 134 |
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~%
2-(4-羟基苯基)噻唑 81015-49-8 |
| 文献:Journal of Medicinal Chemistry, , vol. 29, # 6 p. 1065 - 1080 |
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~%
2-(4-羟基苯基)噻唑 81015-49-8 |
| 文献:Bioorganic and medicinal chemistry, , vol. 11, # 7 p. 1235 - 1246 |
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~%
2-(4-羟基苯基)噻唑 81015-49-8 |
| 文献:Journal of Medicinal Chemistry, , vol. 29, # 6 p. 1065 - 1080 |
| 2-(4-羟基苯基)噻唑上游产品 8 | |
|---|---|
| 2-(4-羟基苯基)噻唑下游产品 0 | |
| 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% |
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实验名称:C. difficile toxins: Counterscreen in absence of substrate UDPG Measured in Biochemic...
来源:Broad Institute
靶标:N/A
External Id:7074-02_Inhibitor_Dose_CherryPick_Activity
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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
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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
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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
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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
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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
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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
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实验名称:C. difficile toxins: HTS for inhibitors of TcdB glycohydrolase activity Measured in B...
来源:Broad Institute
靶标:Toxin B [Clostridium difficile 630]
External Id:7074-01_Inhibitor_Dose_CherryPick_Activity
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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
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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-(2-thiazolyl)phenol |