N-(Pyridin-2-yl)benzamide structure
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Common Name | N-(Pyridin-2-yl)benzamide | ||
|---|---|---|---|---|
| CAS Number | 4589-12-2 | Molecular Weight | 198.22100 | |
| Density | 1.227g/cm3 | Boiling Point | 265.8ºC at 760 mmHg | |
| Molecular Formula | C12H10N2O | Melting Point | 114.5 °C | |
| MSDS | N/A | Flash Point | 114.5ºC | |
| Name | N-pyridin-2-ylbenzamide |
|---|---|
| Synonym | More Synonyms |
| Density | 1.227g/cm3 |
|---|---|
| Boiling Point | 265.8ºC at 760 mmHg |
| Melting Point | 114.5 °C |
| Molecular Formula | C12H10N2O |
| Molecular Weight | 198.22100 |
| Flash Point | 114.5ºC |
| Exact Mass | 198.07900 |
| PSA | 41.99000 |
| LogP | 2.40690 |
| Index of Refraction | 1.65 |
| InChIKey | LZIJKEIPCFEOLH-UHFFFAOYSA-N |
| SMILES | O=C(Nc1ccccn1)c1ccccc1 |
| Storage condition | 2-8°C |
| HS Code | 2933399090 |
|---|
| Precursor 10 | |
|---|---|
| DownStream 3 | |
| HS Code | 2933399090 |
|---|---|
| Summary | 2933399090. other compounds containing an unfused pyridine 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
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Name: Selectivity index, ratio of IC50 for HEK293 cells to IC50 for Trypanosoma brucei bruc...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3371076
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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: Antimicrobial activity against bloodstream form of Trypanosoma brucei brucei 427 afte...
Source: ChEMBL
Target: Trypanosoma brucei brucei
External Id: CHEMBL3371074
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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: 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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| N-(pyridin-2-yl)benzamide |
| Benzamide,N-2-pyridinyl |
| N-(2-pyridinyl)benzamide |
| F3332-0073 |
| 2-(benzoylamino)pyridine |
| N-pyridin-2-ylbenzamine |
| N-(pyrid-2-yl)benzamide |