2-(2-苯并噻唑甲氧基)乙酸结构式
|
常用名 | 2-(2-苯并噻唑甲氧基)乙酸 | 英文名 | 2-(1,3-benzothiazol-2-ylmethoxy)acetic acid |
|---|---|---|---|---|
| CAS号 | 99513-52-7 | 分子量 | 223.24800 | |
| 密度 | N/A | 沸点 | 435.4ºC at 760mmHg | |
| 分子式 | C10H9NO3S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 217.1ºC |
| 中文名 | 2-(2-苯并噻唑甲氧基)乙酸 |
|---|---|
| 英文名 | 2-(1,3-benzothiazol-2-ylmethoxy)acetic acid |
| 英文别名 | 更多 |
| 沸点 | 435.4ºC at 760mmHg |
|---|---|
| 分子式 | C10H9NO3S |
| 分子量 | 223.24800 |
| 闪点 | 217.1ºC |
| 精确质量 | 223.03000 |
| PSA | 87.66000 |
| LogP | 1.89750 |
| InChIKey | RQFMQUWXKKGYMC-UHFFFAOYSA-N |
| SMILES | O=C(O)COCc1nc2ccccc2s1 |
| 海关编码 | 2934200090 |
|---|
|
~%
2-(2-苯并噻唑甲氧基)乙酸 99513-52-7 |
| 文献:Sb. Statei Obshch. Khim., , p. 1096,1097 Chem.Abstr., , p. 5441 |
|
~%
2-(2-苯并噻唑甲氧基)乙酸 99513-52-7 |
| 文献:Sb. Statei Obshch. Khim., , p. 1096,1097 Chem.Abstr., , p. 5441 |
|
~%
2-(2-苯并噻唑甲氧基)乙酸 99513-52-7 |
| 文献:Ukrainskii Khimicheskii Zhurnal (Russian Edition), , vol. 22, p. 208,211 Chem.Abstr., , p. 373 |
|
~%
2-(2-苯并噻唑甲氧基)乙酸 99513-52-7 |
| 文献:Ukrainskii Khimicheskii Zhurnal (Russian Edition), , vol. 22, p. 208,211 Chem.Abstr., , p. 373 |
| 2-(2-苯并噻唑甲氧基)乙酸上游产品 6 | |
|---|---|
| 2-(2-苯并噻唑甲氧基)乙酸下游产品 0 | |
| 海关编码 | 2934200090 |
|---|---|
| 中文概述 | 2934200090. 其他含一个苯并噻唑环系的化合物. 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 | 2934200090. other compounds containing in the structure a benzothiazole ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
|
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
|
|
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
|
|
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: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: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
|
|
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
|
|
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
|
| Benzothiazol-2-ylmethoxy-essigsaeure |
| benzothiazol-2-ylmethoxy-acetic acid |
| HMS2744K17 |
| F1901-0105 |