2-氨基-苯并[b]噻吩-3-羧酸乙酯结构式
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常用名 | 2-氨基-苯并[b]噻吩-3-羧酸乙酯 | 英文名 | Ethyl 2-amino-1-benzothiophene-3-carboxylate |
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| CAS号 | 7311-95-7 | 分子量 | 221.275 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 373.4±22.0 °C at 760 mmHg | |
| 分子式 | C11H11NO2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 179.6±22.3 °C |
| 中文名 | 2-氨基-苯并[B]噻吩-3-羧酸乙酯 |
|---|---|
| 英文名 | ethyl 2-amino-1-benzothiophene-3-carboxylate |
| 英文别名 | 更多 |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 373.4±22.0 °C at 760 mmHg |
| 分子式 | C11H11NO2S |
| 分子量 | 221.275 |
| 闪点 | 179.6±22.3 °C |
| 精确质量 | 221.051056 |
| PSA | 80.56000 |
| LogP | 4.13 |
| InChIKey | XNASJEQIJMDBQN-UHFFFAOYSA-N |
| SMILES | CCOC(=O)c1c(N)sc2ccccc12 |
| 蒸汽压 | 0.0±0.8 mmHg at 25°C |
| 折射率 | 1.666 |
| 储存条件 | 2-8°C,避光,干燥,密封 |
| 危害码 (欧洲) | Xi |
|---|---|
| 海关编码 | 2934999090 |
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~82%
2-氨基-苯并[b]噻吩-3-羧酸乙酯 7311-95-7 |
| 文献:SMITHKLINE BEECHAM CORPORATION Patent: WO2003/104219 A1, 2003 ; Location in patent: Page 10; 12-13 ; WO 03/104219 A1 |
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~60%
2-氨基-苯并[b]噻吩-3-羧酸乙酯 7311-95-7 |
| 文献:Banhegyi, Peter; Gyoergy, Keri; Oerfi, Laszlõ; Szekelyhidi, Zsolt; Waczek, Frigyes Patent: US2011/15214 A1, 2011 ; Location in patent: Page/Page column 8 ; US 20110015214 A1 |
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~34%
2-氨基-苯并[b]噻吩-3-羧酸乙酯 7311-95-7 |
| 文献:BAYER PHARMACEUTICALS CORPORATION Patent: WO2006/44524 A1, 2006 ; Location in patent: Page/Page column 54-55 ; WO 2006/044524 A1 |
| 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:SAR compounds tested by Multiplex dose response to identify specific small molecule i...
来源:NMMLSC
靶标:GTP-binding protein (rab7) [Canis lupus familiaris]
External Id:UNMCMD_Rab7Project_SAR1_Dose_Response_Rab7_wt
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实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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实验名称:Dose Response of round 1 SAR compounds for GTPase inhibitor project tested by multip...
来源:NMMLSC
靶标:N/A
External Id:UNMCMD_Rab7_MgSAR1_Dose_Response_Panel
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实验名称:SAR compounds for Rab7 project tested by Multiplex dose response to identify specific...
来源:NMMLSC
靶标:cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens]
External Id:UNMCMD_Rab7Project_SAR1_Dose_Response_Cdc42_ACT
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实验名称:SAR compounds tested by Multiplex dose response to identify specific small molecule i...
来源:NMMLSC
靶标:cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens]
External Id:UNMCMD_Rab7Project_SAR1_Dose_Response_Cdc42_WT
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实验名称:SAR compounds tested by Multiplex dose response to identify specific small molecule i...
来源:NMMLSC
靶标:ras protein [Homo sapiens]
External Id:UNMCMD_Rab7Project_SAR1_Dose_Response_H-Ras_ACT
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实验名称:SAR compounds tested by Multiplex dose response to identify specific small molecule i...
来源:NMMLSC
靶标:ras protein [Homo sapiens]
External Id:UNMCMD_Rab7Project_SAR1_Dose_Response_Ras_wt
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
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| 2-aminobenzo[b]thiophene-3-carboxylic acid ethyl ester |
| Benzo[b]thiophene-3-carboxylic acid, 2-amino-, ethyl ester |
| 2-amino-benzo<b>thiophene-3-carboxylic acid ethyl esther |
| ethyl 2-aminobenzo(b)thiophene-3-carboxylate |
| Ethyl 2-amino-1-benzothiophene-3-carboxylate |
| 2-amino-3-carbethoxybenzothiophene |
| ethyl-2-amino-benzo(b)thiopene-3-carboxylate |
| 2-aminobenzothiophene-3-carboxylic acid ethyl ester |