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6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid

更新时间:2025-08-26 14:20:01

6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid结构式
6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid结构式
委托求购
常用名 6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid 英文名 6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid
CAS号 6345-59-1 分子量 253.23100
密度 1.65g/cm3 沸点 N/A
分子式 C10H7NO5S 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 6-hydroxy-5-nitrosonaphthalene-2-sulfonic acid
英文别名 更多

 物理化学性质

密度 1.65g/cm3
分子式 C10H7NO5S
分子量 253.23100
精确质量 253.00400
PSA 112.41000
LogP 1.78830
InChIKey ZDPZWHLPCUZHPA-UHFFFAOYSA-N
SMILES O=Nc1c(O)ccc2cc(S(=O)(=O)O)ccc12
折射率 1.693

 合成线路

~%

6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid结构式

6-hydroxy-5-nit...

6345-59-1

文献:Feldmann Giorn.Chim.ind.appl., vol. 7, p. 406 Chem. Zentralbl., 1926 , vol. 97, # I p. 84

~%

6-hydroxy-5-nitroso-naphthalene-2-sulfonic acid结构式

6-hydroxy-5-nit...

6345-59-1

文献:Meldola Journal of the Chemical Society, 1881 , vol. 39, p. 47 Chemische Berichte, 1881 , vol. 14, p. 532

 靶点实验

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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
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: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:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_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: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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 英文别名

5-Hydroxyimino-6-oxo-5,6-dihydro-naphthalin-2-sulfonsaeure
5-hydroxyimino-6-oxo-5,6-dihydro-naphthalene-2-sulfonic acid
HMS3091G18
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