1-(2-苯基-1,3-噻唑-4-基)乙酮结构式
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常用名 | 1-(2-苯基-1,3-噻唑-4-基)乙酮 | 英文名 | 1-(2-Phenyl-1,3-thiazol-4-yl)ethan-1-one |
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| CAS号 | 10045-52-0 | 分子量 | 203.26000 | |
| 密度 | 1.203g/cm3 | 沸点 | 353.5ºC at 760mmHg | |
| 分子式 | C11H9NOS | 熔点 | 84ºC | |
| MSDS | N/A | 闪点 | 167.6ºC |
| 中文名 | 1-(2-苯基-1,3-噻唑-4-基)乙酮 |
|---|---|
| 英文名 | 1-(2-phenyl-1,3-thiazol-4-yl)ethanone |
| 中文别名 | 1-(2-苯基-1,3-噻唑-4-基)-1-乙酮 |
| 英文别名 | 更多 |
| 密度 | 1.203g/cm3 |
|---|---|
| 沸点 | 353.5ºC at 760mmHg |
| 熔点 | 84ºC |
| 分子式 | C11H9NOS |
| 分子量 | 203.26000 |
| 闪点 | 167.6ºC |
| 精确质量 | 203.04000 |
| PSA | 58.20000 |
| LogP | 3.01270 |
| InChIKey | ZOOGZFPRAKXWKI-UHFFFAOYSA-N |
| SMILES | CC(=O)c1csc(-c2ccccc2)n1 |
| 蒸汽压 | 3.58E-05mmHg at 25°C |
| 折射率 | 1.594 |
| 危害码 (欧洲) | Xi: Irritant; |
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| 安全声明 (欧洲) | S24/25 |
| 海关编码 | 2934100090 |
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~97%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:BRISTOL-MYERS SQUIBB COMPANY; UNIVERSITÉ DE MONTRÉAL; BANVILLE, Jacques; RÉMILLARD, Roger; RUEDIGER, Edward H.; DEON, Daniel H.; GAGNON, Marc; DUBÉ, Laurence; GUY, Julia; PRIESTLEY, Eldon Scott; POSY, Shoshana L.; MAXWELL, Brad D.; WONG, Pancras C. Patent: WO2013/163279 A1, 2013 ; Location in patent: Paragraph 00219 ; |
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~86%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:Sarodnick; Kempter Pharmazie, 1983 , vol. 38, # 12 p. 829 - 832 |
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~51%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:Shafiee, A.; Anaraki, M.; Bazzaz, A. Journal of Heterocyclic Chemistry, 1986 , vol. 23, # 3 p. 861 - 864 |
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~%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:Chemische Berichte, , vol. 97, p. 1915 - 1920 |
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~%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:Chemische Berichte, , vol. 97, p. 1915 - 1920 |
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~%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:WO2013/163279 A1, ; |
|
~%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:WO2013/163279 A1, ; |
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~%
1-(2-苯基-1,3-噻唑-... 10045-52-0 |
| 文献:WO2013/163279 A1, ; |
| 1-(2-苯基-1,3-噻唑-4-基)乙酮上游产品 10 | |
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| 1-(2-苯基-1,3-噻唑-4-基)乙酮下游产品 2 | |
| 海关编码 | 2934100090 |
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| 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: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: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:USP8 deubiquitinase inhibition: Primary qHTS
来源:24642
靶标:ubiquitin specific peptidase 8
External Id:USP8 FAST DUB HTS Primary
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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:USP17 deubiquitinase inhibition: Primary qHTS
来源:24642
靶标:ubiquitin specific peptidase 17 like family member 5
External Id:USP17 FAST DUB HTS Primary
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实验名称:USP7 deubiquitinase inhibition: Primary qHTS
来源:24642
靶标:ubiquitin specific peptidase 7
External Id:USP7 FAST DUB HTS Primary
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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
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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.
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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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| 1-(2-phenylthiazol-4-yl)ethanone |
| 5-Acetyl-2-phenylthiohydantoinsaeure |
| 4-Acetyl-2-phenylthiazole |
| 1-(2-Phenylthiazol-4-yl)ethanone |
| 2-Phenyl-4-acetylthiazol |
| 4-acetyl-2-phenyl-1,3-thiazole |
| 1-(2-Phenyl-1,3-thiazol-4-yl)ethan-1-one |