7,8-Dimethyl-4-phenyl-1,3-dihydro-2H-1,5-benzodiazepin-2-one
Modify Date: 2026-07-14 10:54:30
7,8-Dimethyl-4-phenyl-1,3-dihydro-2H-1,5-benzodiazepin-2-one structure
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Common Name | 7,8-Dimethyl-4-phenyl-1,3-dihydro-2H-1,5-benzodiazepin-2-one | ||
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| CAS Number | 82259-42-5 | Molecular Weight | 264.32200 | |
| Density | 1.17g/cm3 | Boiling Point | 471.7ºC at 760 mmHg | |
| Molecular Formula | C17H16N2O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 239.1ºC | |
| Name | 7,8-dimethyl-4-phenyl-1,3-dihydro-1,5-benzodiazepin-2-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.17g/cm3 |
|---|---|
| Boiling Point | 471.7ºC at 760 mmHg |
| Molecular Formula | C17H16N2O |
| Molecular Weight | 264.32200 |
| Flash Point | 239.1ºC |
| Exact Mass | 264.12600 |
| PSA | 41.46000 |
| LogP | 3.34000 |
| Index of Refraction | 1.625 |
| InChIKey | INDZHLYDGYUHKM-UHFFFAOYSA-N |
| SMILES | Cc1cc2c(cc1C)NC(=O)CC(c1ccccc1)=N2 |
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~90%
7,8-Dimethyl-4-... CAS#:82259-42-5 |
| Literature: Bougrin, Khalid; Bennani, A. Kella; Tetouani, Souad Fkih; Soufiaoui, Mohamed Tetrahedron Letters, 1994 , vol. 35, # 45 p. 8373 - 8376 |
| 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: 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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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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| dimethyl-7,8 phenyl-4 dihydro-2,3 benzodiazepine-1,5 one-2 |
| 7,8-Dimethyl-4-phenyl-1,3-dihydro-2H-1,5-benzodiazepin-2-one |
| 2,3-dihydro-7,8-dimethyl-4-phenyl-1H-1,5-benzo-diazepin-2-one |