2-(4-氟苯基)-4H-3,1-苯并恶嗪-4-酮结构式
|
常用名 | 2-(4-氟苯基)-4H-3,1-苯并恶嗪-4-酮 | 英文名 | 2-(4-FLUOROPHENYL)-4H-3,1-BENZOXAZIN-4-ONE |
|---|---|---|---|---|
| CAS号 | 18600-51-6 | 分子量 | 241.21700 | |
| 密度 | 1.31g/cm3 | 沸点 | 343.3ºC at 760mmHg | |
| 分子式 | C14H8FNO2 | 熔点 | 180-181ºC | |
| MSDS | N/A | 闪点 | 161.4ºC |
| 中文名 | 2-(4-氟苯基)-4H-3,1-苯并噁嗪-4-酮 |
|---|---|
| 英文名 | 2-(4-fluorophenyl)-3,1-benzoxazin-4-one |
| 英文别名 | 更多 |
| 密度 | 1.31g/cm3 |
|---|---|
| 沸点 | 343.3ºC at 760mmHg |
| 熔点 | 180-181ºC |
| 分子式 | C14H8FNO2 |
| 分子量 | 241.21700 |
| 闪点 | 161.4ºC |
| 精确质量 | 241.05400 |
| PSA | 43.10000 |
| LogP | 2.99410 |
| InChIKey | FWPIOVHFUGZTPA-UHFFFAOYSA-N |
| SMILES | O=c1oc(-c2ccc(F)cc2)nc2ccccc12 |
| 外观性状 | 固体 |
| 蒸汽压 | 7.1E-05mmHg at 25°C |
| 折射率 | 1.62 |
| 储存条件 | 室温 |
| 危害码 (欧洲) | Xi: Irritant; |
|---|---|
| 海关编码 | 2934999090 |
| 2-(4-氟苯基)-4H-3,1-苯并恶嗪-4-酮上游产品 7 | |
|---|---|
| 2-(4-氟苯基)-4H-3,1-苯并恶嗪-4-酮下游产品 0 | |
| 海关编码 | 2934999090 |
|---|---|
| 中文概述 | 2934999090. 其他杂环化合物. 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 |
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
|
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
|
|
实验名称:Displacement of [3H]DPCPX from Sprague-Dawley rat whole brain membrane A1AR by scinti...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL4625018
|
|
实验名称:Displacement of [3H]NECA from Sprague-Dawley rat striatal membrane A2A adenosine rece...
来源:ChEMBL
靶标:Adenosine receptor A2a
External Id:CHEMBL4625020
|
|
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
|
|
实验名称:Displacement of [3H]DPCPX from Sprague-Dawley rat whole brain membrane A1AR at 100 uM...
来源:ChEMBL
靶标:Adenosine receptor A1
External Id:CHEMBL4625019
|
|
实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
|
|
实验名称:Inhibition of recombinant Escherichia coli N-terminal His-tagged rhomboid protease Gl...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4188950
|
|
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
|
|
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
|
|
实验名称:α-Chymotrypsin Inhibition Kinetic Assay from Article 10.1016/j.bioorg.2017.01.00...
来源:BindingDB
靶标:N/A
External Id:BindingDB_7846_2
|
| fluorophenylbenzoxazinone |
| 2-(4-fluorophenyl)-4H-3,1-benzoxazin-4-one |
| 2-(4-Fluor-phenyl)-4H-3,1-benzoxazinon-(4) |
| 2-(4-fluorophenyl)benzo[d]1,3-oxazin-4-one |
| 2-(4-fluorophenyl)-4H-benzo[d][1,3]oxazin-4-one |
| 2-(4-fluorophenyl)-3,1-benzoxazin-4(3H)-one |
| 2-(p-fluoro-benzyl)-4H-3,1-benzoxazin-4-one |