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N-(4-甲氧基苯基)香豆素-3-甲酰胺

更新时间:2025-10-18 16:47:57

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式
N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式
品牌特惠专场
常用名 N-(4-甲氧基苯基)香豆素-3-甲酰胺 英文名 N-(4-methoxyphenyl)-2-oxo-2H-chromene-3-carboxamide
CAS号 1846-94-2 分子量 295.28900
密度 N/A 沸点 N/A
分子式 C17H13NO4 熔点 N/A
MSDS N/A 闪点 N/A

 N-(4-甲氧基苯基)香豆素-3-甲酰胺名称

中文名 N-(4-甲氧基苯基)香豆素-3-甲酰胺
英文名 N-(4-methoxyphenyl)-2-oxochromene-3-carboxamide
英文别名 更多

 N-(4-甲氧基苯基)香豆素-3-甲酰胺物理化学性质

分子式 C17H13NO4
分子量 295.28900
精确质量 295.08400
PSA 68.54000
LogP 3.12690
InChIKey UVIDYPCYACCLOZ-UHFFFAOYSA-N
SMILES COc1ccc(NC(=O)c2cc3ccccc3oc2=O)cc1

 N-(4-甲氧基苯基)香豆素-3-甲酰胺安全信息

海关编码 2932209090

 N-(4-甲氧基苯基)香豆素-3-甲酰胺合成线路

~70%

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式

N-(4-甲氧基苯基)香豆素-3-甲酰胺

1846-94-2

文献:Bonsignore; Loy; Secci; Calignano European Journal of Medicinal Chemistry, 1993 , vol. 28, # 6 p. 517 - 520

~%

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式

N-(4-甲氧基苯基)香豆素-3-甲酰胺

1846-94-2

文献:Ukhov; Kon'shin; Odegova Pharmaceutical Chemistry Journal, 2001 , vol. 35, # 7 p. 364 - 365

~%

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式

N-(4-甲氧基苯基)香豆素-3-甲酰胺

1846-94-2

文献:Bonsignore, Leonardo; Cabiddu, Salvatore; Loy, Giuseppe; Secci, Mario Heterocycles, 1984 , vol. 22, # 11 p. 2587 - 2590

~%

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式

N-(4-甲氧基苯基)香豆素-3-甲酰胺

1846-94-2

文献:Ukhov; Kon'shin; Odegova Pharmaceutical Chemistry Journal, 2001 , vol. 35, # 7 p. 364 - 365

~%

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式

N-(4-甲氧基苯基)香豆素-3-甲酰胺

1846-94-2

文献:Ukhov; Kon'shin; Odegova Pharmaceutical Chemistry Journal, 2001 , vol. 35, # 7 p. 364 - 365

~%

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式

N-(4-甲氧基苯基)香豆素-3-甲酰胺

1846-94-2

文献:Ichibagase; Terada Yakugaku Zasshi, 1953 , vol. 73, p. 466 Chem.Abstr., 1954 , p. 3356

~%

N-(4-甲氧基苯基)香豆素-3-甲酰胺结构式

N-(4-甲氧基苯基)香豆素-3-甲酰胺

1846-94-2

文献:Kassur; Weil Roczniki Chemii, 1938 , vol. 18, p. 163,166 Chem. Zentralbl., 1939 , vol. 110, # II p. 1491

 N-(4-甲氧基苯基)香豆素-3-甲酰胺海关

海关编码 2932209090
中文概述 2932209090. 其他内酯. 增值税率:17.0%. 退税率:13.0%. 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 2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 N-(4-甲氧基苯基)香豆素-3-甲酰胺靶点实验

查看更多实验

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: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
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
实验名称:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
靶标:HIV-1 Vif
External Id:HIV1-VIF_MS
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 N-(4-甲氧基苯基)香豆素-3-甲酰胺英文别名

2-oxo-2H-chromene-3-carboxylic acid p-anisidide
2-Oxo-2H-chromen-3-carbonsaeure-p-anisidid
Coumarin-3-carbonsaeure-N-<4-methoxy-phenyl>-amid
coumarin-3-carboxylic acid anisidide
3-carboxamido coumarin,16
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