1-丙基-1H-苯并[d]咪唑-2-胺结构式
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常用名 | 1-丙基-1H-苯并[d]咪唑-2-胺 | 英文名 | 1-propyl-1H-benzoimidazol-2-ylamine |
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| CAS号 | 57667-50-2 | 分子量 | 175.23000 | |
| 密度 | 1.18g/cm3 | 沸点 | 349.7ºC at 760mmHg | |
| 分子式 | C10H13N3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 165.3ºC |
| 中文名 | 1-丙基-1H-苯并咪唑-2-胺 |
|---|---|
| 英文名 | 1-propylbenzimidazol-2-amine |
| 英文别名 | 更多 |
| 密度 | 1.18g/cm3 |
|---|---|
| 沸点 | 349.7ºC at 760mmHg |
| 分子式 | C10H13N3 |
| 分子量 | 175.23000 |
| 闪点 | 165.3ºC |
| 精确质量 | 175.11100 |
| PSA | 43.84000 |
| LogP | 2.60970 |
| InChIKey | MGKUHRRJQCKXOW-UHFFFAOYSA-N |
| SMILES | CCCn1c(N)nc2ccccc21 |
| 折射率 | 1.624 |
| 储存条件 | 室温,避光,保存于惰性气体中 |
| 海关编码 | 2933990090 |
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~64%
1-丙基-1H-苯并[d]咪唑-2-胺 57667-50-2 |
| 文献:GLAXOSMITHKLINE LLC; LAFRANCE, Louis, Vincent; LEBER, Jack, Dale; LI, Mei; VERMA, Sharad, Kumar Patent: WO2010/126922 A1, 2010 ; Location in patent: Page/Page column 15 ; WO 2010/126922 A1 |
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~59%
1-丙基-1H-苯并[d]咪唑-2-胺 57667-50-2 |
| 文献:Di Braccio, Mario; Grossi, Giancarlo; Signorello, Maria Grazia; Leoncini, Giuliana; Cichero, Elena; Fossa, Paola; Alfei, Silvana; Damonte, Gianluca European Journal of Medicinal Chemistry, 2013 , vol. 62, p. 564 - 578 |
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1-丙基-1H-苯并[d]咪唑-2-胺 57667-50-2 |
| 文献:Bioorganic and Medicinal Chemistry Letters, , vol. 18, # 7 p. 2414 - 2419 |
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1-丙基-1H-苯并[d]咪唑-2-胺 57667-50-2 |
| 文献:European Journal of Medicinal Chemistry, , vol. 41, # 9 p. 1080 - 1083 |
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1-丙基-1H-苯并[d]咪唑-2-胺 57667-50-2 |
| 文献:Bioorganic and Medicinal Chemistry, , vol. 15, # 18 p. 6291 - 6297 |
| 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: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: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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| 1-propylbenzimidazole-2-ylamine |
| MFCD00964693 |
| 1-Propyl-1H-benzoimidazol-2-ylamine |
| 2-Amino-1-propyl-benzimidazol |
| F2124-0423 |
| 1-propyl-1H-benzimidazol-2-amine |
| 2-amino-1-propyl-1H-benzimidazole |