5-Methoxy-1,2,3-triazine

ALDRICH/ALD00500

Empirical Formula (Hill Notation): C₄H₅N₃O
Molecular Weight: 111.10
Linear Formula: C₄H₅N₃O
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-ALD00500-100MG	100 mg	$498.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

form	powder
InChI	1S/C4H5N3O/c1-8-4-2-5-7-6-3-4/h2-3H,1H3
InChI key	HVBZCUMRMKODNE-UHFFFAOYSA-N
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

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