(4-氯苄基)-吡啶-2-胺双盐酸盐结构式
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常用名 | (4-氯苄基)-吡啶-2-胺双盐酸盐 | 英文名 | 2-Pyridinamine,N-[(4-chlorophenyl)methyl] |
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| CAS号 | 22881-33-0 | 分子量 | 218.68200 | |
| 密度 | 1.251g/cm3 | 沸点 | 351.7ºC at 760mmHg | |
| 分子式 | C12H11ClN2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 166.5ºC |
| 中文名 | (4-氯苄基)-吡啶-2-胺双盐酸盐 |
|---|---|
| 英文名 | (4-chloro-benzyl)-pyridin-2-yl-amine dihydrochloride |
| 密度 | 1.251g/cm3 |
|---|---|
| 沸点 | 351.7ºC at 760mmHg |
| 分子式 | C12H11ClN2 |
| 分子量 | 218.68200 |
| 闪点 | 166.5ºC |
| 精确质量 | 218.06100 |
| PSA | 24.92000 |
| LogP | 3.42010 |
| InChIKey | QCRNCCIQUTVWLT-UHFFFAOYSA-N |
| SMILES | Clc1ccc(CNc2ccccn2)cc1 |
| 蒸汽压 | 4.04E-05mmHg at 25°C |
| 折射率 | 1.644 |
| 海关编码 | 2933399090 |
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~86%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Cano, Rafael; Yus, Miguel; Ramon, Diego J. Tetrahedron, 2011 , vol. 67, # 42 p. 8079 - 8085 |
|
~88%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Tetrahedron Letters, , vol. 51, # 2 p. 325 - 327 |
|
~%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Organic Letters, , vol. 15, # 13 p. 3476 - 3479 |
|
~%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Organic Letters, , vol. 15, # 13 p. 3476 - 3479 |
|
~44%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Fioravanti; Biava; Donnarumma; Porretta; Simonetti; Villa; Porta-Puglia; Deidda; Maullu; Pompei Farmaco, 1996 , vol. 51, # 10 p. 643 - 652 |
|
~99%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Cano, Rafael; Ramon, Diego J.; Yus, Miguel Journal of Organic Chemistry, 2011 , vol. 76, # 14 p. 5547 - 5557 |
|
~%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Organic Letters, , vol. 15, # 13 p. 3476 - 3479 |
|
~%
(4-氯苄基)-吡啶-2-胺双盐酸盐 22881-33-0 |
| 文献:Farmaco, , vol. 51, # 10 p. 643 - 652 |
| (4-氯苄基)-吡啶-2-胺双盐酸盐上游产品 5 | |
|---|---|
| (4-氯苄基)-吡啶-2-胺双盐酸盐下游产品 1 | |
| 海关编码 | 2933399090 |
|---|---|
| 中文概述 | 2933399090. 其他结构含非稠合吡啶环的化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. 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: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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