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Spiro(3.3)heptane-2,6-dicarboxamide

更新时间:2025-08-20 12:19:47

Spiro(3.3)heptane-2,6-dicarboxamide结构式
Spiro(3.3)heptane-2,6-dicarboxamide结构式
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常用名 Spiro(3.3)heptane-2,6-dicarboxamide 英文名 Spiro(3.3)heptane-2,6-dicarboxamide
CAS号 707-45-9 分子量 182.22000
密度 1.27g/cm3 沸点 506.5ºC at 760 mmHg
分子式 C9H14N2O2 熔点 N/A
MSDS N/A 闪点 260.1ºC

 Spiro(3.3)heptane-2,6-dicarboxamide名称

英文名 spiro[3.3]heptane-2,6-dicarboxamide
英文别名 更多

 Spiro(3.3)heptane-2,6-dicarboxamide物理化学性质

密度 1.27g/cm3
沸点 506.5ºC at 760 mmHg
分子式 C9H14N2O2
分子量 182.22000
闪点 260.1ºC
精确质量 182.10600
PSA 86.18000
LogP 1.16400
InChIKey ACKODFNIGGGCBA-UHFFFAOYSA-N
SMILES NC(=O)C1CC2(C1)CC(C(N)=O)C2
折射率 1.57

 Spiro(3.3)heptane-2,6-dicarboxamide合成线路

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Spiro(3.3)heptane-2,6-dicarboxamide结构式

Spiro(3.3)hepta...

707-45-9

文献:Rice,L.M.; Grogan,C.H. Journal of Organic Chemistry, 1961 , vol. 26, p. 54 - 58

 Spiro(3.3)heptane-2,6-dicarboxamide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: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
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 Spiro(3.3)heptane-2,6-dicarboxamide英文别名

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