5-Methoxy-1,2,3-triazine
ALDRICH/ALD00500
Empirical Formula (Hill Notation): C4H5N3O
Molecular Weight: 111.10
MDL Number: MFCD29917853
Linear Formula: C4H5N3O
Product Type: Chemical
| form | powder |
| InChI | 1S/C4H5N3O/c1-8-4-2-5-7-6 |
| InChI key | HVBZCUMRMKODNE-UHFFFAOYSA |
| Quality Level | 100 ![]() |
| SMILES string | COC1=CN=NN=C1 |
| storage temp. | 2-8°C |
| Application: | 1, 2, 3-Triazines have shown to be reactive substrates in inverse electron demand Diels-Alder strategies. Recent examples by Boger and coworkers utilize this reactive motif in the construction of highly functionalized N-containing heterocycles. |
| Application: | 5-Methoxy-1,2,3-triazine may be used in the synthesis of nitrogen-containing heterocyclic compounds. |
| General description: | 5-Methoxy-1,2,3-triazine is a 1,2,3-triazine derivative bearing electron-donating substituent. It participates in the inverse electron demand Diels-Alder reactions. 5-Methoxy-1,2,3-triazine readily reacts with amidines. It can be prepared from 4-methoxypyrazole. |
| Legal Information: | Cycloadditions of 1,2,3-Triazines Bearing C5-Electron Donating Substituents: Robust Pyrimidine Synthesis ![]() |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | 2-8°C |
| UNSPSC | 12352100 |

