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3-[(4-hydroxyphenyl)amino]-5,5-dimethyl-cyclohex-2-en-1-one

更新时间:2025-08-26 03:20:28

3-[(4-hydroxyphenyl)amino]-5,5-dimethyl-cyclohex-2-en-1-one结构式
3-[(4-hydroxyphenyl)amino]-5,5-dimethyl-cyclohex-2-en-1-one结构式
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常用名 3-[(4-hydroxyphenyl)amino]-5,5-dimethyl-cyclohex-2-en-1-one 英文名 3-[(4-hydroxyphenyl)amino]-5,5-dimethyl-cyclohex-2-en-1-one
CAS号 50685-30-8 分子量 231.29000
密度 1.179g/cm3 沸点 386.4ºC at 760 mmHg
分子式 C14H17NO2 熔点 N/A
MSDS N/A 闪点 187.5ºC

 名称

英文名 3-(4-hydroxyanilino)-5,5-dimethylcyclohex-2-en-1-one
英文别名 更多

 物理化学性质

密度 1.179g/cm3
沸点 386.4ºC at 760 mmHg
分子式 C14H17NO2
分子量 231.29000
闪点 187.5ºC
精确质量 231.12600
PSA 49.33000
LogP 3.15010
InChIKey YOXNZHPNAXSUNO-UHFFFAOYSA-N
SMILES CC1(C)CC(=O)C=C(Nc2ccc(O)cc2)C1
折射率 1.608

 上下游产品

上游产品  2

下游产品  0

 靶点实验

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实验名称:C. difficile toxins: Counterscreen in absence of substrate UDPG Measured in Biochemic...
来源:Broad Institute
靶标:N/A
External Id:7074-02_Inhibitor_Dose_CherryPick_Activity
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: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
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
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
实验名称:C. difficile toxins: HTS for inhibitors of TcdB glycohydrolase activity Measured in B...
来源:Broad Institute
靶标:Toxin B [Clostridium difficile 630]
External Id:7074-01_Inhibitor_Dose_CherryPick_Activity
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: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
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 英文别名

3-p-Hydroxyanilino-5,5-dimethyl-2-cyclohexenon
3-(4-Hydroxy-phenylamino)-5,5-dimethyl-cyclohex-2-enone
3-[(4-hydroxyphenyl)amino]-5,5-dimethylcyclohex-2-en-1-one
5.5-Dimethyl-3-(4'-hydroxyanilino)cyclohex-2-en-1-on
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