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7-Hydroxy-5-methyl-1,3,4-triazaindolizine

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7-Hydroxy-5-methyl-1,3,4-triazaindolizine Basic information

Product Name:
7-Hydroxy-5-methyl-1,3,4-triazaindolizine
Synonyms:
  • 2,4]Triazolo[1,5-a]pyrimidin-7-ol,5-methyl-[1
  • 5-a)pyrimidin-7-ol,5-methyl-s-triazolo(
  • 5-Methyl-7-hydroxy-1,3,4-triazindolizine
  • 5-Methyl-s-trazolo[1,5-]pyrimidin-7-ol
  • Methyl hydroxytriazaindolizine
  • 5-Methyl-s-triazolo[1,5-a]pyrimidin-7-ol,98%
  • 5-Methyl (1,2,4)trizolo(1,5-α)pyrimidin-7-ol
  • 5-Methyl-[1,2,4]triazolo[1,5-a]pyridin-7-ol
CAS:
2503-56-2
MF:
C6H6N4O
MW:
150.14
EINECS:
219-706-7
Product Categories:
  • Industrial/Fine Chemicals
  • Benzotriazoles
  • Building Blocks
  • C-C Bond Formation
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Others
  • Synthetic Reagents
Mol File:
2503-56-2.mol
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7-Hydroxy-5-methyl-1,3,4-triazaindolizine Chemical Properties

Melting point:
280-283 °C(lit.)
Boiling point:
271.66°C (rough estimate)
Density 
1.3471 (rough estimate)
vapor pressure 
0-0Pa at 20-25℃
refractive index 
1.6700 (estimate)
storage temp. 
2-8°C
pka
1.14±0.53(Predicted)
color 
White to Almost white
Water Solubility 
INSOLUBLE IN COLD WATER
BRN 
609440
InChIKey
ZUIVNYGZFPOXFW-UHFFFAOYSA-N
LogP
-1.4 at 19℃ and pH7.1
CAS DataBase Reference
2503-56-2(CAS DataBase Reference)
NIST Chemistry Reference
Pyrimidin-7-ol, 5-methyl-s-triazolo-[1,5-a]-(2503-56-2)
EPA Substance Registry System
[1,2,4]Triazolo[1,5-a]pyrimidin-7-ol, 5-methyl- (2503-56-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
1
RTECS 
XZ6133300
9
Hazard Note 
Harmful
TSCA 
Yes
HS Code 
2933998090
Toxicity
mouse,LD50,intravenous,> 450mg/kg (450mg/kg),Oyo Yakuri. Pharmacometrics. Vol. 13, Pg. 597, 1977.

MSDS

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7-Hydroxy-5-methyl-1,3,4-triazaindolizine Usage And Synthesis

Chemical Properties

7-Hydroxy-5-methyl-1,3,4-triazaindolizine is white fine crystalline powder

Uses

Reactant for the synthesis of: • ;Ruthenium(II)-Hmtpo complexes1• ;Dihydroorotate dehydrogenase inhibitors with antimalarial activity2Reactant for the Vilsmeier reaction of conjugated carbocycles and heterocycles3Investigations of the pharmacological activity caused by binding to HIV TAR RNA4Additive to study the space charge layer in silver bromide microcrystals5

Uses

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

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