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3-(1-(2,6-DICHLORO-3-FLUOROPHENYL)ETHOXY)-5-(1-(PIPERIDIN-4-YL)-1H-PYRAZOL-4-YL)PYRIDIN-2-AMINE

更新时间:2025-09-12 14:07:55

3-(1-(2,6-DICHLORO-3-FLUOROPHENYL)ETHOXY)-5-(1-(PIPERIDIN-4-YL)-1H-PYRAZOL-4-YL)PYRIDIN-2-AMINE结构式
3-(1-(2,6-DICHLORO-3-FLUOROPHENYL)ETHOXY)-5-(1-(PIPERIDIN-4-YL)-1H-PYRAZOL-4-YL)PYRIDIN-2-AMINE结构式
品牌特惠专场
常用名 3-(1-(2,6-DICHLORO-3-FLUOROPHENYL)ETHOXY)-5-(1-(PIPERIDIN-4-YL)-1H-PYRAZOL-4-YL)PYRIDIN-2-AMINE 英文名 3-(1-(2,6-DICHLORO-3-FLUOROPHENYL)ETHOXY)-5-(1-(PIPERIDIN-4-YL)-1H-PYRAZOL-4-YL)PYRIDIN-2-AMINE
CAS号 877400-66-3 分子量 450.33700
密度 1.475g/cm3 沸点 599.177ºC at 760 mmHg
分子式 C21H22Cl2FN5O 熔点 N/A
MSDS N/A 闪点 316.171ºC

 名称

英文名 3-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-(1-piperidin-4-ylpyrazol-4-yl)pyridin-2-amine
英文别名 更多

 物理化学性质

密度 1.475g/cm3
沸点 599.177ºC at 760 mmHg
分子式 C21H22Cl2FN5O
分子量 450.33700
闪点 316.171ºC
精确质量 449.11900
PSA 77.99000
LogP 5.94770
InChIKey KTEIFNKAUNYNJU-UHFFFAOYSA-N
SMILES CC(Oc1cc(-c2cnn(C3CCNCC3)c2)cnc1N)c1c(Cl)ccc(F)c1Cl
折射率 1.673

 安全信息

海关编码 2933990090

 海关

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%

 靶点实验

查看更多实验

实验名称:Inhibition of human recombinant c-MET kinase expressed in A549 cells assessed as inhi...
来源:ChEMBL
靶标:Hepatocyte growth factor receptor
External Id:CHEMBL1826482
实验名称:Drug screen in LFS_MB_P medulloblastoma cells to determine synergistic drug combinati...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_LFS_MB_P
实验名称:Inhibition of recombinant GST-tagged ALK L1196M mutant (1064 to 1427 residues) (unkno...
来源:ChEMBL
靶标:ALK tyrosine kinase receptor
External Id:CHEMBL5140257
实验名称:Drug screen in ICB984 medulloblastoma cells to determine synergistic drug combination...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_ICB984_MB
实验名称: Inhibitory Activity Against Anaplastic Lymphoma Kinase (ALK) from US Patent US100534...
来源:BindingDB
靶标:N/A
External Id:BindingDB_237_1
实验名称:Inhibition of recombinant GST-tagged wild type ALK (1064 to 1427 residues) (unknown o...
来源:ChEMBL
靶标:ALK tyrosine kinase receptor
External Id:CHEMBL5140258
实验名称:Drug screen in HDN33 neuroblastoma cells to determine synergistic drug combinations t...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_HDN33
实验名称:Binding affinity to human recombinant c-MET assessed as inhibition of autophosphoryla...
来源:ChEMBL
靶标:Hepatocyte growth factor receptor
External Id:CHEMBL1825352
实验名称:Drug screen in HD-MB03 medulloblastoma cells to determine synergistic drug combinatio...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_HD-MB03
实验名称:Metabolic stability in human liver microsome assessed as compound remaining after 30 ...
来源:ChEMBL
靶标:Liver microsomes
External Id:CHEMBL1825353
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 英文别名

(R)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)pyridin-2-amine
3-(1-(2,6-dichloro-3-fluoro-phenyl)ethoxy)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-amine
Kinome_3145
Kinome_3144
Kinome_3143
BOCCHEM BC-L-Y016
2-PYRIDINAMINE,3-[1-(2,6-DICHLORO-3-FLUOROPHENYL)ETHOXY]-5-[1-(4-PIPERIDINYL)-1H-PYRAZOL-4-YL]
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