(5-氯-1H-苯并咪唑-2-基)乙酸结构式
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常用名 | (5-氯-1H-苯并咪唑-2-基)乙酸 | 英文名 | 2-(5-CHLORO-1H-BENZO[D]IMIDAZOL-2-YL)ACETIC ACID |
|---|---|---|---|---|
| CAS号 | 53350-32-6 | 分子量 | 210.61700 | |
| 密度 | 1.566g/cm3 | 沸点 | 525.3ºC at 760 mmHg | |
| 分子式 | C9H7ClN2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 271.5ºC |
| 中文名 | (5-氯-1H-苯并咪唑-2-基)乙酸 |
|---|---|
| 英文名 | 2-(6-chloro-1H-benzimidazol-2-yl)acetic acid |
| 英文别名 | 更多 |
| 密度 | 1.566g/cm3 |
|---|---|
| 沸点 | 525.3ºC at 760 mmHg |
| 分子式 | C9H7ClN2O2 |
| 分子量 | 210.61700 |
| 闪点 | 271.5ºC |
| 精确质量 | 210.02000 |
| PSA | 65.98000 |
| LogP | 1.84340 |
| InChIKey | DHHUPGJLPIWIGU-UHFFFAOYSA-N |
| SMILES | O=C(O)Cc1nc2ccc(Cl)cc2[nH]1 |
| 折射率 | 1.711 |
| 危害码 (欧洲) | Xi |
|---|---|
| 海关编码 | 2933990090 |
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~%
(5-氯-1H-苯并咪唑-2-基)乙酸 53350-32-6 |
| 文献:US3933847 A1, ; |
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~70%
(5-氯-1H-苯并咪唑-2-基)乙酸 53350-32-6 |
| 文献:Essassi, E. M.; Lamkadem, A.; Zniber, R. Bulletin des Societes Chimiques Belges, 1991 , vol. 100, # 3 p. 277 - 286 |
| (5-氯-1H-苯并咪唑-2-基)乙酸上游产品 3 | |
|---|---|
| (5-氯-1H-苯并咪唑-2-基)乙酸下游产品 0 | |
| 海关编码 | 2933990090 |
|---|---|
| 中文概述 | 2933990090. 其他仅含氮杂原子的杂环化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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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:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
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实验名称:Inhibitors of CDC25B-CDK2/CyclinA interaction
来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
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实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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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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实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
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| Acide chloro-5 benzimidazolyl-2 acetique |