Quinoxaline, 1,4-diacetyl-1,2,3,4-tetrahydro- (9CI)
Modify Date: 2025-11-25 15:25:06
Quinoxaline, 1,4-diacetyl-1,2,3,4-tetrahydro- (9CI) structure
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Common Name | Quinoxaline, 1,4-diacetyl-1,2,3,4-tetrahydro- (9CI) | ||
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| CAS Number | 7151-45-3 | Molecular Weight | 218.25200 | |
| Density | 1.206g/cm3 | Boiling Point | 516.3ºC at 760mmHg | |
| Molecular Formula | C12H14N2O2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 267.1ºC | |
| Name | 1-(4-acetyl-2,3-dihydroquinoxalin-1-yl)ethanone |
|---|---|
| Synonym | More Synonyms |
| Density | 1.206g/cm3 |
|---|---|
| Boiling Point | 516.3ºC at 760mmHg |
| Molecular Formula | C12H14N2O2 |
| Molecular Weight | 218.25200 |
| Flash Point | 267.1ºC |
| Exact Mass | 218.10600 |
| PSA | 40.62000 |
| LogP | 1.53600 |
| Index of Refraction | 1.57 |
| InChIKey | XCSRFSPPKXTWFD-UHFFFAOYSA-N |
| SMILES | CC(=O)N1CCN(C(C)=O)c2ccccc21 |
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Quinoxaline, 1,... CAS#:7151-45-3 |
| Literature: Ris Chemische Berichte, 1888 , vol. 21, p. 378 |
| Precursor 2 | |
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| DownStream 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: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
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| 1,4-Diacetyl-1,2,3,4-tetrahydro-chinoxalin |
| 1,4-Diacetoxy-pentan |
| 1,4-diacetyl-1,2,3,4-tetrahydroquinoxaline |
| 1,4-Pentanediol,diacetate |
| 1,4-diacetoxypentane |