3,4-二氢-2(1H)-喹啉酮结构式
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常用名 | 3,4-二氢-2(1H)-喹啉酮 | 英文名 | 3,4-Dihydroquinolin-2(1H)-one |
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| CAS号 | 553-03-7 | 分子量 | 147.174 | |
| 密度 | 1.1±0.1 g/cm3 | 沸点 | 328.1±31.0 °C at 760 mmHg | |
| 分子式 | C9H9NO | 熔点 | 165-167ºC | |
| MSDS | 美版 | 闪点 | 189.4±9.8 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
| 中文名 | 3,4-二氢-2(1H)-喹啉酮 |
|---|---|
| 英文名 | 1,2,3,4-Tetrahydroquinolin-2-one |
| 中文别名 | 鄰胺氫桂皮酸內醯胺 | 2-氧-1,2,3,4-四氫喹啉 | 3,4-二氫-2(1H)-喹啉酮 | 氢化喹诺酮 |
| 英文别名 | 更多 |
| 密度 | 1.1±0.1 g/cm3 |
|---|---|
| 沸点 | 328.1±31.0 °C at 760 mmHg |
| 熔点 | 165-167ºC |
| 分子式 | C9H9NO |
| 分子量 | 147.174 |
| 闪点 | 189.4±9.8 °C |
| 精确质量 | 147.068420 |
| PSA | 29.10000 |
| LogP | 1.34 |
| InChIKey | TZOYXRMEFDYWDQ-UHFFFAOYSA-N |
| SMILES | O=C1CCc2ccccc2N1 |
| 外观性状 | 灰白色结晶粉末 |
| 蒸汽压 | 0.0±0.7 mmHg at 25°C |
| 折射率 | 1.564 |
| 储存条件 | 室温 |
| 符号 |
GHS07 |
|---|---|
| 信号词 | Warning |
| 危害声明 | H302-H315-H317-H319-H335 |
| 警示性声明 | P261-P280-P305 + P351 + P338 |
| 危害码 (欧洲) | Xn:Harmful; |
| 风险声明 (欧洲) | R22;R36/37/38;R43 |
| 安全声明 (欧洲) | S26-S36/37 |
| 危险品运输编码 | UN 2811 |
| WGK德国 | 2 |
| 包装等级 | III |
| 危险类别 | 6.1(b) |
| 3,4-二氢-2(1H)-喹啉酮上游产品 10 | |
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| 3,4-二氢-2(1H)-喹啉酮下游产品 10 | |
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Synthesis and biological evaluation of a novel sigma-1 receptor antagonist based on 3,4-dihydro-2(1H)-quinolinone scaffold as a potential analgesic.
Eur. J. Med. Chem. 79 , 216-30, (2014) The synthesis and sigma-1 receptor (1R) antagonist activity of a new series of 3,4-dihydro-2(1H)-quinolinone derivatives are reported. The new compounds were evaluated in vitro in sigma-1 and sigma-2 ... |
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Novel approach to 3,4-dihydro-2(1H)-quinolinone derivatives via cyclopropane ring expansion.
Org. Lett. 11(5) , 1043-5, (2009) N-(1'-Alkoxy)cyclopropyl-2-haloanilines are transformed to 3,4-dihydro-2((1)H)-quinolinones via palladium-catalyzed cyclopropane ring expansion. The reaction tolerates a variety of functional groups s... |
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Synthesis of 4-amino-3, 4-dihydro-2 (1H)-quinolinones via β-lactam intermediates on the solid-phase. Pei Y, et al.
Tetrahedron Lett. 38(19) , 3349-52, (1997)
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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:Inhibition of transglutaminase in human keratinocytes in presence of 10 uM retinal re...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4420714
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| Dihydro-α-quinolone |
| 3,4-Dihydroquinolin-2(1H)-one |
| 3,4-dihydro-1H-quinolin-2-one |
| MFCD00016722 |
| 3,4-Dihydro-2(1H)-quinolinone |
| T66 BMVT&J |