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2',4'-二羟基苯丁酮

更新时间:2025-08-26 23:01:30

2',4'-二羟基苯丁酮结构式
2',4'-二羟基苯丁酮结构式
品牌特惠专场
常用名 2',4'-二羟基苯丁酮 英文名 1-Butanone,1-(2,4-dihydroxyphenyl)
CAS号 4390-92-5 分子量 180.201
密度 1.2±0.1 g/cm3 沸点 338.5±12.0 °C at 760 mmHg
分子式 C10H12O3 熔点 N/A
MSDS N/A 闪点 172.7±16.1 °C

 2',4'-二羟基苯丁酮名称

中文名 2’,4’-二羟基苯丁酮
英文名 1-(2,4-dihydroxyphenyl)butan-1-one
中文别名 2',4'-二羟基苯丁酮 | 1-(2,4-二羟基-苯基)-1-丁酮
英文别名 更多

 2',4'-二羟基苯丁酮物理化学性质

密度 1.2±0.1 g/cm3
沸点 338.5±12.0 °C at 760 mmHg
分子式 C10H12O3
分子量 180.201
闪点 172.7±16.1 °C
精确质量 180.078644
PSA 57.53000
LogP 2.80
InChIKey IWADIQGGJLCBRK-UHFFFAOYSA-N
SMILES CCCC(=O)c1ccc(O)cc1O
蒸汽压 0.0±0.8 mmHg at 25°C
折射率 1.567
储存条件 室温,干燥密封

 2',4'-二羟基苯丁酮合成线路

~%

2',4'-二羟基苯丁酮结构式

2',4'-二羟基苯丁酮

4390-92-5

文献:Nakazawa Yakugaku Zasshi, 1954 , vol. 74, p. 836 Chem.Abstr., 1955 , p. 9556 Full Text Show Details Oelschlaeger Archiv der Pharmazie (Weinheim, Germany), 1955 , vol. 288, p. 102,107,108

~69%

2',4'-二羟基苯丁酮结构式

2',4'-二羟基苯丁酮

4390-92-5

文献:Mizobuchi, Shigeyuki; Sato, Yuko Agricultural and Biological Chemistry, 1985 , vol. 49, # 5 p. 1327 - 1334

~%

2',4'-二羟基苯丁酮结构式

2',4'-二羟基苯丁酮

4390-92-5

文献:Astill et al. Biochemical Journal, 1959 , vol. 72, p. 451,457

~%

2',4'-二羟基苯丁酮结构式

2',4'-二羟基苯丁酮

4390-92-5

文献:Desai; Mavani Proceedings - Indian Academy of Sciences, Section A, 1949 , vol. 29, p. 269,270

~%

2',4'-二羟基苯丁酮结构式

2',4'-二羟基苯丁酮

4390-92-5

文献:Jin, Can; Li, Jie; Su, Weike Journal of Chemical Research, 2009 , # 10 p. 607 - 611

~%

2',4'-二羟基苯丁酮结构式

2',4'-二羟基苯丁酮

4390-92-5

文献:Booth, Brian L.; Noori, Ghazi F.M. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2894 - 2900

~%

2',4'-二羟基苯丁酮结构式

2',4'-二羟基苯丁酮

4390-92-5

文献:Desai; Mavani Proceedings - Indian Academy of Sciences, Section A, 1949 , vol. 29, p. 269,270

 2',4'-二羟基苯丁酮靶点实验

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:qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2
来源:NCGC
靶标:eyes absent homolog 2 isoform a [Homo sapiens]
External Id:EYA2477
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: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: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
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 2',4'-二羟基苯丁酮英文别名

1-(2,4-dihydroxy-phenyl)-butan-1-one
1-(2,4-Dihydroxyphenyl)-1-butanone
2,4-dihydroxyphenyl propyl ketone
1-(2,4-Dihydroxy-phenyl)-butan-1-on
1-(2,4-dihydroxyphenyl)butanone
1-(2,4-dihydroxyphenyl)butan-1-one
2,4-dihydroxybutyrophenone
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