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177679 Sigma-Aldrich

7-Hydroxy-5-methyl[1,2,4]triazolo[1,5-a]pyrimidine

98%

Synonym: 5-Methyl[1,2,4]triazolo[1,5-a]pyrimidin-7-ol, 6-Methyl-4-hydroxy-1,3,3a,7-tetraazaindene, 7-Hydroxy-5-methyl-1,3,4-triazaindolizine, NSC 32071, NSC 511493

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Properties

Related Categories Benzotriazoles, Building Blocks, C-C Bond Formation, Chemical Synthesis, Heterocyclic Building Blocks,
assay   98%
reaction suitability   reaction type: C-C Bond Formation
mp   280-283 °C (lit.)
SMILES string   Cc1cc(O)n2ncnc2n1
InChI   1S/C6H6N4O/c1-4-2-5(11)10-6(9-4)7-3-8-10/h2-3,11H,1H3
InChI key   ZUIVNYGZFPOXFW-UHFFFAOYSA-N

Description

Application

Reactant for the synthesis of:
• Ruthenium(II)-Hmtpo complexes
• Dihydroorotate dehydrogenase inhibitors with antimalarial activity

Reactant for the Vilsmeier reaction of conjugated carbocycles and heterocycles

Investigations of the pharmacological activity caused by binding to HIV TAR RNA

Additive to study the space charge layer in silver bromide microcrystals

Packaging

25 g in poly bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
1
RTECS 
XZ6133300
Protocols & Articles
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