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Benzeneacetic acid, a-(1-hydroxy-4-methylcyclohexyl)

更新时间:2025-08-31 16:02:06

Benzeneacetic acid, a-(1-hydroxy-4-methylcyclohexyl)结构式
Benzeneacetic acid, a-(1-hydroxy-4-methylcyclohexyl)结构式
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常用名 Benzeneacetic acid, a-(1-hydroxy-4-methylcyclohexyl) 英文名 Benzeneacetic acid, a-(1-hydroxy-4-methylcyclohexyl)
CAS号 5449-33-2 分子量 248.31700
密度 1.171g/cm3 沸点 401.9ºC at 760mmHg
分子式 C15H20O3 熔点 N/A
MSDS N/A 闪点 211ºC

 名称

英文名 2-(1-hydroxy-4-methylcyclohexyl)-2-phenylacetic acid
英文别名 更多

 物理化学性质

密度 1.171g/cm3
沸点 401.9ºC at 760mmHg
分子式 C15H20O3
分子量 248.31700
闪点 211ºC
精确质量 248.14100
PSA 57.53000
LogP 2.79600
InChIKey YYQPXJFURRUIAG-UHFFFAOYSA-N
SMILES CC1CCC(O)(C(C(=O)O)c2ccccc2)CC1
折射率 1.566

 合成线路

~%

Benzeneacetic acid, a-(1-hydroxy-4-methylcyclohexyl)结构式

Benzeneacetic a...

5449-33-2

文献:Treves; Testa Journal of the American Chemical Society, 1952 , vol. 74, p. 46

~%

Benzeneacetic acid, a-(1-hydroxy-4-methylcyclohexyl)结构式

Benzeneacetic a...

5449-33-2

文献:Blicke, Arbor Patent: US2922795 , 1960 ; Chem.Abstr., 1960 , vol. 54, # 19453

 靶点实验

查看更多实验

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: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: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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
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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 英文别名

(1-hydroxy-4-methyl-cyclohexyl)-phenyl-acetic acid
(1-Hydroxy-4-methyl-cyclohexyl)-phenyl-essigsaeure
HMS3087K18
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