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3,4-二氢-2(1H)-喹啉酮

更新时间:2025-08-22 22:02:33

3,4-二氢-2(1H)-喹啉酮结构式
3,4-二氢-2(1H)-喹啉酮结构式
品牌特惠专场
常用名 3,4-二氢-2(1H)-喹啉酮 英文名 3,4-Dihydroquinolin-2(1H)-one
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
GHS07
信号词 Warning

 3,4-二氢-2(1H)-喹啉酮名称

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

 3,4-二氢-2(1H)-喹啉酮物理化学性质

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

 3,4-二氢-2(1H)-喹啉酮MSDS

 3,4-二氢-2(1H)-喹啉酮安全信息

符号 GHS07
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)-喹啉酮合成线路

 3,4-二氢-2(1H)-喹啉酮文献4

更多文献
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 ...

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...

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)

 3,4-二氢-2(1H)-喹啉酮靶点实验

查看更多实验

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
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
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
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
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
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: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.
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
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
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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 3,4-二氢-2(1H)-喹啉酮英文别名

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
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