7-Ethyl-1H-indole-2,3-dione
Modify Date: 2026-08-05 20:59:47
7-Ethyl-1H-indole-2,3-dione structure
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Common Name | 7-Ethyl-1H-indole-2,3-dione | ||
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| CAS Number | 79183-65-6 | Molecular Weight | 175.18400 | |
| Density | 1.247g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C10H9NO2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 7-Ethylindoline-2,3-dione |
|---|---|
| Synonym | More Synonyms |
| Density | 1.247g/cm3 |
|---|---|
| Molecular Formula | C10H9NO2 |
| Molecular Weight | 175.18400 |
| Exact Mass | 175.06300 |
| PSA | 46.17000 |
| LogP | 1.52180 |
| Index of Refraction | 1.583 |
| InChIKey | YMZGAPGIOFRUFU-UHFFFAOYSA-N |
| SMILES | CCc1cccc2c1NC(=O)C2=O |
| HS Code | 2933990090 |
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~83%
7-Ethyl-1H-indo... CAS#:79183-65-6 |
| Literature: Yamamoto, Gaku; Koseki, Ai; Sugita, Jun; Mochida, Hisashi; Minoura, Mao Bulletin of the Chemical Society of Japan, 2006 , vol. 79, # 10 p. 1585 - 1600 |
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7-Ethyl-1H-indo... CAS#:79183-65-6 |
| Literature: Journal of Medicinal Chemistry, , vol. 50, # 1 p. 21 - 39 |
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7-Ethyl-1H-indo... CAS#:79183-65-6 |
| Literature: Journal of the Chemical Society, , p. 3095 |
![(E)-[(dimethoxyphosphinyl)oxy]-1,2-dimethylethylene structure](https://image.chemsrc.com/caspic/497/50522-37-7.png)
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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|
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
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|
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: 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
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Name: High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
Target: N/A
External Id: HMS1149-MLP
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Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
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| 7-ethyl-1H-indole-2,3-dione |