2-Oxazolidinone,3-phenyl-5-[(2-propyn-1-yloxy)methyl]结构式
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常用名 | 2-Oxazolidinone,3-phenyl-5-[(2-propyn-1-yloxy)methyl] | 英文名 | 2-Oxazolidinone,3-phenyl-5-[(2-propyn-1-yloxy)methyl] |
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| CAS号 | 23598-54-1 | 分子量 | 231.24700 | |
| 密度 | 1.203g/cm3 | 沸点 | 353.3ºC at 760mmHg | |
| 分子式 | C13H13NO3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 167.5ºC |
| 英文名 | 3-phenyl-5-(prop-2-ynoxymethyl)-1,3-oxazolidin-2-one |
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| 英文别名 | 更多 |
| 密度 | 1.203g/cm3 |
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| 沸点 | 353.3ºC at 760mmHg |
| 分子式 | C13H13NO3 |
| 分子量 | 231.24700 |
| 闪点 | 167.5ºC |
| 精确质量 | 231.09000 |
| PSA | 38.77000 |
| LogP | 1.72660 |
| InChIKey | RXVDTRQMYILFDO-UHFFFAOYSA-N |
| SMILES | C#CCOCC1CN(c2ccccc2)C(=O)O1 |
| 蒸汽压 | 3.61E-05mmHg at 25°C |
| 折射率 | 1.555 |
| 海关编码 | 2934999090 |
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2-Oxazolidinone... 23598-54-1 |
| 文献:Fugitt; Martinelli Journal of pharmaceutical sciences, 1973 , vol. 62, # 6 p. 1013 - 1016 |
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2-Oxazolidinone... 23598-54-1 |
| 文献:Fauron,C.; Douzon,C. Chimica Therapeutica, 1973 , vol. 8, p. 143 - 147 |
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~%
2-Oxazolidinone... 23598-54-1 |
| 文献:Fauron,C.; Douzon,C. Chimica Therapeutica, 1973 , vol. 8, p. 143 - 147 |
|
~%
2-Oxazolidinone... 23598-54-1 |
| 文献:Fauron,C.; Douzon,C. Chimica Therapeutica, 1973 , vol. 8, p. 143 - 147 |
|
~%
2-Oxazolidinone... 23598-54-1 |
| 文献:Fauron,C.; Douzon,C. Chimica Therapeutica, 1973 , vol. 8, p. 143 - 147 |
|
~%
2-Oxazolidinone... 23598-54-1 |
| 文献:Fauron,C.; Douzon,C. Chimica Therapeutica, 1973 , vol. 8, p. 143 - 147 |
|
~%
2-Oxazolidinone... 23598-54-1 |
| 文献:Fauron,C.; Douzon,C. Chimica Therapeutica, 1973 , vol. 8, p. 143 - 147 |
| 海关编码 | 2934999090 |
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| 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% |
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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:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
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实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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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:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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| 3-phenyl-5-prop-2-ynyloxymethyl-oxazolidin-2-one |
| 2-Oxazolidinone,3-phenyl-5-[(2-propynyloxy)methyl] |
| N-Phenyl-5-propargyloxymethyloxazolidin-2-on |
| 2-oxazolidinone,3-phenyl-5-[(2-propyn-1-yloxy)methyl] |
| 3-Phenyl-5-(2-propynyloxymethyl)-2-oxazolidinone |