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1H-BENZOTRIAZOLE-1-METHANOL

1H-BENZOTRIAZOLE-1-METHANOL Structure
CAS No.
28539-02-8
Chemical Name:
1H-BENZOTRIAZOLE-1-METHANOL
Synonyms
NSC 12463;AKOS 92621;AURORA 19841;Benzotriazolemethanol;1-Benzotriazolemethanol;BENZOTRIAZOL-1-YL-METHANOL;1H-BENZOTRIAZOLE-1-METHANOL;1H-Benzotriazol-1-ylmethanol;1-HydroxyMethyl benzotriazole;1H-Benzotriazole-1-Methanol 98%
CBNumber:
CB3267637
Molecular Formula:
C7H7N3O
Molecular Weight:
149.15
MOL File:
28539-02-8.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

1H-BENZOTRIAZOLE-1-METHANOL 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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  2933998090

1H-BENZOTRIAZOLE-1-METHANOL price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 410233 1H-Benzotriazole-1-methanol 98% 28539-02-8 10G ₹3312.45 2022-06-14 Buy
Sigma-Aldrich(India) 410233 1H-Benzotriazole-1-methanol 98% 28539-02-8 50G ₹16194.2 2022-06-14 Buy
TCI Chemicals (India) B1903 1H-Benzotriazole-1-methanol min. 95.0 % 28539-02-8 25G ₹6300 2022-05-26 Buy
Product number Packaging Price Buy
410233 10G ₹3312.45 Buy
410233 50G ₹16194.2 Buy
B1903 25G ₹6300 Buy

1H-BENZOTRIAZOLE-1-METHANOL Chemical Properties,Uses,Production

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

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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 (1H-benzo[d][1,2,3]triazol-1-yl)Methanol 1H-Benzotriazole-1-Methanol 98% 1-Benzotriazolemethanol NSC 12463 Benzotriazolemethanol (1H-Benzotriazole-1-yl)methanol 1H-Benzotriazole-1-methanol > 28539-02-8 ALCOHOL C-C Bond Formation Others Synthetic Reagents C-C Bond Formation Others Synthetic Reagents