1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐结构式
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常用名 | 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐 | 英文名 | 4-Piperidone, 1-hydroxy-2,2,6,6-tetramethyl |
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| CAS号 | 3637-11-4 | 分子量 | 171.23700 | |
| 密度 | 1.02g/cm3 | 沸点 | 257.5ºC at 760mmHg | |
| 分子式 | C9H17NO2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 109.5ºC |
1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐用途Tempone-H可用作化学和生物系统中的自旋陷阱,以量化过亚硝酸根和超氧自由基的形成。铁离子和铜离子是Tempone-H[1][2]的有效氧化剂。 |
| 中文名 | 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐 |
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| 英文名 | 1-hydroxy-2,2,6,6-tetramethylpiperidin-4-one |
| 英文别名 | 更多 |
| 描述 | Tempone-H可用作化学和生物系统中的自旋陷阱,以量化过亚硝酸根和超氧自由基的形成。铁离子和铜离子是Tempone-H[1][2]的有效氧化剂。 |
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| 相关类别 | |
| 体外研究 | 使用TEMPONE-H检测过氧亚硝酸盐或超氧自由基的灵敏度约为使用自旋陷阱DMPO或TMIO的10倍[1]。 |
| 参考文献 |
| 密度 | 1.02g/cm3 |
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| 沸点 | 257.5ºC at 760mmHg |
| 分子式 | C9H17NO2 |
| 分子量 | 171.23700 |
| 闪点 | 109.5ºC |
| 精确质量 | 171.12600 |
| PSA | 40.54000 |
| LogP | 1.53560 |
| InChIKey | KMEUSKGEUADGET-UHFFFAOYSA-N |
| SMILES | CC1(C)CC(=O)CC(C)(C)N1O |
| 储存条件 | -20°C |
| 海关编码 | 2933399090 |
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| 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐上游产品 8 | |
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| 1-羟基-2,2,6,6-四甲基-4-氧-哌啶盐酸盐下游产品 3 | |
| 海关编码 | 2933399090 |
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| 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: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:Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4296184
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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:Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA...
来源:ChEMBL
靶标:Escherichia coli
External Id:CHEMBL4296185
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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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| 1-hydroxy-2,2,6,6-tetramethyl-piperidin-4-one |
| 1-Hydroxy-2,2,6,6-tetramethyl-4-oxopiperidine |
| 4-oxo-TEMPO-H |
| 4-Piperidinone,1-hydroxy-2,2,6,6-tetramethyl |
| 1-Hydroxy-2,2,6,6-tetramethyl-piperidin-4-on |
| 2,2,6,6-tetramethyl-4-oxo-1-piperidinyloxy |
| Tempone-H |
| N-hydroxy-4-oxo-2,2,6,6-tetramethylpiperidine |
| 1-Hydroxy-2,2,6,6-tetramethyl-4-piperidinone |