| Identification | More | [Name]
1H-BENZOTRIAZOLE-1-METHANOL | [CAS]
28539-02-8 | [Synonyms]
1H-1,2,3-BENZOTRIAZOL-1-YLMETHANOL
1H-BENZOTRIAZOLE-1-METHANOL
1-(HYDROXYMETHYL)-1H-BENZOTRIAZOLE
AKOS 92621
AURORA 19841
BENZOTRIAZOL-1-YL-METHANOL
Benzotriazolemethanol
(1H-Benzotriazole-1-yl)methanol | [Molecular Formula]
C7H7N3O | [MDL Number]
MFCD00179118 | [Molecular Weight]
149.15 | [MOL File]
28539-02-8.mol |
| Chemical Properties | Back Directory | [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) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [HS Code ]
2933998090 |
| Hazard Information | Back Directory | [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
| [reaction suitability]
reaction type: C-C Bond Formation |
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