4-Bromo-5-nitro-1H-imidazole
Modify Date: 2026-08-05 22:48:07
4-Bromo-5-nitro-1H-imidazole structure
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Common Name | 4-Bromo-5-nitro-1H-imidazole | ||
|---|---|---|---|---|
| CAS Number | 6963-65-1 | Molecular Weight | 191.971 | |
| Density | 2.2±0.1 g/cm3 | Boiling Point | 382.2±22.0 °C at 760 mmHg | |
| Molecular Formula | C3H2BrN3O2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 184.9±22.3 °C | |
| Name | 5-bromo-4-nitro-1h-imidazole |
|---|---|
| Synonym | More Synonyms |
| Density | 2.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 382.2±22.0 °C at 760 mmHg |
| Molecular Formula | C3H2BrN3O2 |
| Molecular Weight | 191.971 |
| Flash Point | 184.9±22.3 °C |
| Exact Mass | 190.933029 |
| PSA | 74.50000 |
| LogP | 0.85 |
| Vapour Pressure | 0.0±0.8 mmHg at 25°C |
| Index of Refraction | 1.664 |
| InChIKey | KSEFBYAEHWXHLM-UHFFFAOYSA-N |
| SMILES | O=[N+]([O-])c1[nH]cnc1Br |
| Hazard Codes | Xn |
|---|---|
| HS Code | 2933290090 |
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4-Bromo-5-nitro... CAS#:6963-65-1 |
| Literature: Pratt, John K.; Betebenner, David A.; Donner, Pemela L.; Green, Brian E.; Kempf, Dale J.; McDaniel, Keith F.; Maring, Clarence J.; Stoll, Vincent S.; Zhang, Rong Patent: US2004/87577 A1, 2004 ; Location in patent: Page 122-123 ; |
| HS Code | 2933290090 |
|---|---|
| Summary | 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) 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
|
|
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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| 4(5)-Bromo-5(4)-nitroimidazole |
| 5-Bromo-4-nitroimidazole |
| 4-Bromo-5-nitro-1H-imidazole |
| 4-bromo-5-nitro-1(3)H-imidazole |
| 5-bromo-5-nitroimidazole |
| 4-Brom-5-nitro-imidazol |
| 4-bromo-5-nitroimidazole |
| 5(4)-bromo-4(5)-nitroimidazole |