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1H-BENZOTRIAZOLE-1-METHANOL

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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
Product Categories:
  • C-C Bond Formation
  • Others
  • Synthetic Reagents
Mol File:
28539-02-8.mol
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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
pka
12.80±0.10(Predicted)
color 
White to Almost white
InChIKey
MXJIHEXYGRXHGP-UHFFFAOYSA-N
CAS DataBase Reference
28539-02-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2933998090

MSDS

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1H-BENZOTRIAZOLE-1-METHANOL Usage And Synthesis

Uses

Catalyst 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

1H-BENZOTRIAZOLE-1-METHANOLSupplier

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