5-(3-氯苯基)-呋喃-2-羧酸结构式
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常用名 | 5-(3-氯苯基)-呋喃-2-羧酸 | 英文名 | 5-(3-chloro-phenyl)-furan-2-carboxylic acid |
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| CAS号 | 41019-44-7 | 分子量 | 222.62400 | |
| 密度 | 1.374g/cm3 | 沸点 | 398.6ºC at 760 mmHg | |
| 分子式 | C11H7ClO3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 194.9ºC |
| 中文名 | 5-(3-氯苯基)呋喃-2-羧酸 |
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| 英文名 | 5-(3-chlorophenyl)furan-2-carboxylic acid |
| 英文别名 | 更多 |
| 密度 | 1.374g/cm3 |
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| 沸点 | 398.6ºC at 760 mmHg |
| 分子式 | C11H7ClO3 |
| 分子量 | 222.62400 |
| 闪点 | 194.9ºC |
| 精确质量 | 222.00800 |
| PSA | 50.44000 |
| LogP | 3.29820 |
| InChIKey | OWEBZHHXEPQWQW-UHFFFAOYSA-N |
| SMILES | O=C(O)c1ccc(-c2cccc(Cl)c2)o1 |
| 折射率 | 1.594 |
| 储存条件 | 2-8°C, 密封, 干燥, 避光 |
| 危害码 (欧洲) | Xi |
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| 海关编码 | 2932190090 |
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~97%
5-(3-氯苯基)-呋喃-2-羧酸 41019-44-7 |
| 文献:Murasawa, Shinpei; Sato, Shinichi; Noguchi-Yachide, Tomomi; Hashimoto, Yuichi; Iuchi, Katsuya; Sodeoka, Mikiko; Dodo, Kosuke; Yokomatsu, Tsutomu; Aoyama, Hiroshi Bioorganic and Medicinal Chemistry, 2012 , vol. 20, # 21 p. 6384 - 6393,10 |
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~87%
5-(3-氯苯基)-呋喃-2-羧酸 41019-44-7 |
| 文献:Ballard, T. Eric; Wang, Xia; Olekhnovich, Igor; Koerner, Taylor; Seymour, Craig; Salamoun, Joseph; Warthan, Michelle; Hoffman, Paul S.; Macdonald, Timothy L. ChemMedChem, 2011 , vol. 6, # 2 p. 362 - 377 |
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~%
5-(3-氯苯基)-呋喃-2-羧酸 41019-44-7 |
| 文献:Denonne, Frederic; Binet, Sophie; Burton, Maggi; Collart, Philippe; Dipesa, Alan; Ganguly, Tanmoy; Giannaras, Alexander; Kumar, Seema; Lewis, Timothy; Maounis, Florence; Nicolas, Jean-Marie; Mansley, Tamsin; Pasau, Patrick; Preda, Dorin; Stebbins, Karin; Volosov, Alexander; Zou, Dong Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 12 p. 3258 - 3261 |
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~%
5-(3-氯苯基)-呋喃-2-羧酸 41019-44-7 |
| 文献:Denonne, Frederic; Binet, Sophie; Burton, Maggi; Collart, Philippe; Dipesa, Alan; Ganguly, Tanmoy; Giannaras, Alexander; Kumar, Seema; Lewis, Timothy; Maounis, Florence; Nicolas, Jean-Marie; Mansley, Tamsin; Pasau, Patrick; Preda, Dorin; Stebbins, Karin; Volosov, Alexander; Zou, Dong Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 12 p. 3258 - 3261 |
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~%
5-(3-氯苯基)-呋喃-2-羧酸 41019-44-7 |
| 文献:Liu, Shu; Premnath, Padmavathy Nandha; Bolger, Joshua K.; Perkins, Tracy L.; Kirkland, Lindsay O.; Kontopidis, George; McInnes, Campbell Journal of Medicinal Chemistry, 2013 , vol. 56, # 4 p. 1573 - 1582 |
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~%
5-(3-氯苯基)-呋喃-2-羧酸 41019-44-7 |
| 文献:Ballard, T. Eric; Wang, Xia; Olekhnovich, Igor; Koerner, Taylor; Seymour, Craig; Salamoun, Joseph; Warthan, Michelle; Hoffman, Paul S.; Macdonald, Timothy L. ChemMedChem, 2011 , vol. 6, # 2 p. 362 - 377 |
| 5-(3-氯苯基)-呋喃-2-羧酸上游产品 6 | |
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| 5-(3-氯苯基)-呋喃-2-羧酸下游产品 2 | |
| 海关编码 | 2932190090 |
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| 中文概述 | 2932190090 其他结构上有非稠合呋喃环化合物. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:6.5% 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| Summary | 2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
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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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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| MFCD02067340 |