1H-BENZOTRIAZOLE-1-METHANOL
1H-BENZOTRIAZOLE-1-METHANOL
  • CAS No.:28539-02-8
Other grades of this product :
1H-BENZOTRIAZOLE-1-METHANOL Basic information
Product Name:1H-BENZOTRIAZOLE-1-METHANOL
Synonyms:BENZOTRIAZOL-1-YL-METHANOL;AURORA 19841;AKOS 92621;1H-1,2,3-BENZOTRIAZOL-1-YLMETHANOL;1H-BENZOTRIAZOLE-1-METHANOL;1-(HYDROXYMETHYL)-1H-BENZOTRIAZOLE;1H-Benzotriazol-1-ylmethanol;1-HydroxyMethyl benzotriazole
CAS:28539-02-8
MF:C7H7N3O
MW:149.15
EINECS:
Product Categories:C-C Bond Formation;Others;Synthetic Reagents
Mol File:28539-02-8.mol
1H-BENZOTRIAZOLE-1-METHANOL Chemical Properties
Melting point 150-152 °C (lit.)
Boiling point 340.2±25.0 °C(Predicted)
density 1.41±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form powder to crystal
pka12.80±0.10(Predicted)
color White to Almost white
InChIKeyMXJIHEXYGRXHGP-UHFFFAOYSA-N
CAS DataBase Reference28539-02-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2933998090
MSDS Information
ProviderLanguage
SigmaAldrich English
1H-BENZOTRIAZOLE-1-METHANOL Usage And Synthesis
UsesCatalyst for:
  • Hydrolysis of phenyl esters of a-furoic acid
Used as:
  • Corrosion inhibitor of iron in aerated acidic media
  • Reactive oxygen scavenger
Reactant for:
  • Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation
  • Enantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement
  • Synthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitors
  • Gosteli-Claisen rearrangement

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