4-甲基-2-(2-噻吩基)-1,3-噻唑-5-羧酸乙酯结构式
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常用名 | 4-甲基-2-(2-噻吩基)-1,3-噻唑-5-羧酸乙酯 | 英文名 | Ethyl4-Methyl-2-(thiophen-2-yl)thiazole-5-carboxylate |
|---|---|---|---|---|
| CAS号 | 56421-62-6 | 分子量 | 253.340 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 380.9±50.0 °C at 760 mmHg | |
| 分子式 | C11H11NO2S2 | 熔点 | 66-68ºC | |
| MSDS | N/A | 闪点 | 184.1±30.1 °C | |
| 符号 |
GHS05 |
信号词 | Danger |
用途ethyl 4-methyl-2-(2-thienyl)-thiazole-5 Carboxylate is a synthetic intermediate useful for pharmaceutical synthesis. |
| 中文名 | 4-甲基-2-(2-噻吩基)噻唑-5-羧酸乙酯 |
|---|---|
| 英文名 | ethyl 4-methyl-2-thiophen-2-yl-1,3-thiazole-5-carboxylate |
| 英文别名 | 更多 |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 380.9±50.0 °C at 760 mmHg |
| 熔点 | 66-68ºC |
| 分子式 | C11H11NO2S2 |
| 分子量 | 253.340 |
| 闪点 | 184.1±30.1 °C |
| 精确质量 | 253.023117 |
| PSA | 95.67000 |
| LogP | 3.81 |
| InChIKey | NRTAQEAHFFIBFX-UHFFFAOYSA-N |
| SMILES | CCOC(=O)c1sc(-c2cccs2)nc1C |
| 蒸汽压 | 0.0±0.9 mmHg at 25°C |
| 折射率 | 1.593 |
| 储存条件 | -20°C,密闭,干燥 |
| 符号 |
GHS05 |
|---|---|
| 信号词 | Danger |
| 危害声明 | H318 |
| 警示性声明 | P280-P305 + P351 + P338 |
| 危险品运输编码 | NONH for all modes of transport |
| 海关编码 | 2934999090 |
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4-甲基-2-(2-噻吩基)-... 56421-62-6 |
| 文献:Journal of Organic Chemistry, , vol. 40, p. 3183 - 3189 |
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4-甲基-2-(2-噻吩基)-... 56421-62-6 |
| 文献:Bioorganic and Medicinal Chemistry Letters, , vol. 20, # 9 p. 2828 - 2831 |
| 4-甲基-2-(2-噻吩基)-1,3-噻唑-5-羧酸乙酯上游产品 4 | |
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| 4-甲基-2-(2-噻吩基)-1,3-噻唑-5-羧酸乙酯下游产品 0 | |
| 海关编码 | 2934999090 |
|---|---|
| 中文概述 | 2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 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 | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . 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: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: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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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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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
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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| 5-Thiazolecarboxylic acid, 4-methyl-2-(2-thienyl)-, ethyl ester |
| 4-methyl-2-thiophen-2-yl-thiazole-5-carboxylic acid ethyl ester |
| Ethyl 4-methyl-2-(2-thienyl)-1,3-thiazole-5-carboxylate |
| 2'-(4-Methyl-5-carbethoxy-2-thiazolyl)-thiophen |
| ethyl 4-methyl-2-(thiophen-2-yl)-1,3-thiazole-5-carboxylate |