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2H-1,3-Benzoxazine-2,4(3H)-dione,3-methyl

更新时间:2025-08-25 20:22:30

2H-1,3-Benzoxazine-2,4(3H)-dione,3-methyl结构式
2H-1,3-Benzoxazine-2,4(3H)-dione,3-methyl结构式
委托求购
常用名 2H-1,3-Benzoxazine-2,4(3H)-dione,3-methyl 英文名 2H-1,3-Benzoxazine-2,4(3H)-dione,3-methyl
CAS号 1672-01-1 分子量 177.15700
密度 1.348g/cm3 沸点 297.5ºC at 760mmHg
分子式 C9H7NO3 熔点 N/A
MSDS N/A 闪点 133.7ºC

 名称

英文名 3-methyl-1,3-benzoxazine-2,4-dione
英文别名 更多

 物理化学性质

密度 1.348g/cm3
沸点 297.5ºC at 760mmHg
分子式 C9H7NO3
分子量 177.15700
闪点 133.7ºC
精确质量 177.04300
PSA 52.21000
LogP 0.49170
InChIKey FBZWKVSQOBDAQR-UHFFFAOYSA-N
SMILES Cn1c(=O)oc2ccccc2c1=O
蒸汽压 0.00135mmHg at 25°C
折射率 1.583

 安全信息

海关编码 2934999090

 合成线路

 海关

海关编码 2934999090
中文概述 2934999090. 其他杂环化合物. 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 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 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: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: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
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 英文别名

2H-1,4(3H)-dione,3-methyl
3,4-Dihydro-3-methyl-2H-1,3-benzoxazine-2,4-dione
3-methyl-benz[e][1,3]oxazine-2,4-dione
3-Methyl-benz[e][1,3]oxazin-2,4-dion
3-methyl-benzo[e][1,3]oxazine-2,4-dione
2H-1,3-Benzoxazine-2,4(3H)-dione,3-methyl
HMS3080N04
N-methyl-1,3-benzoxazine-2,4-dione
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