2-(1H-四唑-1-基)苯甲酸结构式
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常用名 | 2-(1H-四唑-1-基)苯甲酸 | 英文名 | 2-(tetrazol-1-yl)benzoic acid |
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| CAS号 | 116570-12-8 | 分子量 | 190.15900 | |
| 密度 | 1.53g/cm3 | 沸点 | 428.9ºC at 760mmHg | |
| 分子式 | C8H6N4O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 213.2ºC |
| 中文名 | 2-(1H-四唑-1-基)苯甲酸 |
|---|---|
| 英文名 | 2-(tetrazol-1-yl)benzoic acid |
| 中文别名 | 2,6-二乙基吡啶 |
| 英文别名 | 更多 |
| 密度 | 1.53g/cm3 |
|---|---|
| 沸点 | 428.9ºC at 760mmHg |
| 分子式 | C8H6N4O2 |
| 分子量 | 190.15900 |
| 闪点 | 213.2ºC |
| 精确质量 | 190.04900 |
| PSA | 80.90000 |
| LogP | 0.36050 |
| InChIKey | BHBFPWBHORPKDU-UHFFFAOYSA-N |
| SMILES | O=C(O)c1ccccc1-n1cnnn1 |
| 蒸汽压 | 4.03E-08mmHg at 25°C |
| 海关编码 | 2933990090 |
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2-(1H-四唑-1-基)苯甲酸 116570-12-8 |
| 文献:Barrow, James C.; Coburn, Craig; Selnick, Harold G.; Ngo, Phung L. Patent: US2002/193398 A1, 2002 ; US 20020193398 A1 |
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2-(1H-四唑-1-基)苯甲酸 116570-12-8 |
| 文献:Aridoss, Gopalakrishnan; Laali, Kenneth K. European Journal of Organic Chemistry, 2011 , # 15 p. 2827 - 2835 |
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2-(1H-四唑-1-基)苯甲酸 116570-12-8 |
| 文献:GLAXO GROUP LIMITED Patent: WO2006/67462 A1, 2006 ; Location in patent: Page/Page column 58 ; WO 2006/067462 A1 |
| 海关编码 | 2933990090 |
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| 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: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: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: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: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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| 2,6-DIETHYLPYRIDINE |
| 1-<2-Carboxy-phenyl>-tetrazol |
| 2-Tetrazol-1-yl-benzoic acid |