2,4(1H,3H)-Pyrimidinedione,5-bromodihydro-1-(phenylmethyl)
Modify Date: 2026-08-03 20:01:04
2,4(1H,3H)-Pyrimidinedione,5-bromodihydro-1-(phenylmethyl) structure
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Common Name | 2,4(1H,3H)-Pyrimidinedione,5-bromodihydro-1-(phenylmethyl) | ||
|---|---|---|---|---|
| CAS Number | 3959-45-3 | Molecular Weight | 283.12100 | |
| Density | 1.579g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C11H11BrN2O2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 1-benzyl-5-bromo-1,3-diazinane-2,4-dione |
|---|---|
| Synonym | More Synonyms |
| Density | 1.579g/cm3 |
|---|---|
| Molecular Formula | C11H11BrN2O2 |
| Molecular Weight | 283.12100 |
| Exact Mass | 282.00000 |
| PSA | 49.41000 |
| LogP | 1.76860 |
| Index of Refraction | 1.615 |
| InChIKey | RSAIQVSFFIVXNW-UHFFFAOYSA-N |
| SMILES | O=C1NC(=O)N(Cc2ccccc2)CC1Br |
| HS Code | 2933599090 |
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~27%
2,4(1H,3H)-Pyri... CAS#:3959-45-3 |
| Literature: QUEEN'S UNIVERSITY AT KINGSTON Patent: WO2004/9559 A2, 2004 ; Location in patent: Page 34 ; |
| Precursor 1 | |
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| DownStream 0 | |
| HS Code | 2933599090 |
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| Summary | 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. 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: 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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Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
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| HMS3092J07 |
| 1-Benzyl-5-brom-dihydro-pyrimidin-2,4-dion |
| 1-benzyl-5-bromo-dihydro-pyrimidine-2,4-dione |