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benzo[c]xanthen-7-one

更新时间:2025-08-25 19:04:31

benzo[c]xanthen-7-one结构式
benzo[c]xanthen-7-one结构式
委托求购
常用名 benzo[c]xanthen-7-one 英文名 benzo[c]xanthen-7-one
CAS号 63154-69-8 分子量 246.26000
密度 1.312g/cm3 沸点 448.957ºC at 760 mmHg
分子式 C17H10O2 熔点 N/A
MSDS N/A 闪点 218.541ºC

 benzo[c]xanthen-7-one名称

英文名 benzo[c]xanthen-7-one
英文别名 更多

 benzo[c]xanthen-7-one物理化学性质

密度 1.312g/cm3
沸点 448.957ºC at 760 mmHg
分子式 C17H10O2
分子量 246.26000
闪点 218.541ºC
精确质量 246.06800
PSA 30.21000
LogP 4.09940
InChIKey IIEFLOYQNMSGDX-UHFFFAOYSA-N
SMILES O=c1c2ccccc2oc2c1ccc1ccccc12
折射率 1.71

 benzo[c]xanthen-7-one安全信息

海关编码 2932999099

 benzo[c]xanthen-7-one合成线路

 benzo[c]xanthen-7-one海关

海关编码 2932999099
中文概述 2932999099. 其他仅含氧杂原子的杂环化合物. 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 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 benzo[c]xanthen-7-one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: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: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: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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 benzo[c]xanthen-7-one英文别名

3,4-benzoxanthone
HMS3096O12
benzo[c]xanthone
Benzo[c]xanthen-7-on
3:4-Benzo-xanthon
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