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CAS RN: 26456-05-3 | Product Number: M1787

10-Methylacridinium Perchlorate


Purity: >98.0%(N)
Synonyms:
Product Documents:
250MG
€51.00
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1G
€166.00
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Product Number M1787
Purity / Analysis Method >98.0%(N)
Molecular Formula / Molecular Weight C__1__4H__1__2ClNO__4 = 293.70 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
Packaging and Container 1G-Glass Bottle with Plastic Insert (View image)
CAS RN 26456-05-3
Reaxys Registry Number 3647072
PubChem Substance ID 87559032
Specifications
Appearance Light yellow to Amber to Dark green powder to crystal
Purity(with Total Nitrogen) min. 98.0 %
Properties (reference)
Melting Point 241 °C(dec.)
GHS
Pictogram Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
H272 : May intensify fire; oxidizer.
Precautionary Statements P220 : Keep away from clothing and other combustible materials.
P210 : Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
Related Laws:
Transport Information:
UN Number UN1479
Class 5.1
Packing Group III
HS Number 2933998090
Application
Baeyer–Villiger Oxidation with 10-Methylacridinium as an Organocatalyst

Typical Procedure:
Cyclobutanone (0.5 mmol) and 10-methylacridinium perchlorate (7.4 mg, 0.025 mmol) are dissolved in CH3CN (1 mL). Hydrogen peroxide (68 µL, 30% solution in water, 0.6 mmol) is added and the mixture is irradiated with a 450 W high-pressure mercury lamp in a Pyrex® flask (λ>320 nm) at room temperature for 20 h. The course of the reaction is monitored by TLC. After completion of the reaction, solvent is evaporated in vacuum. Purification of the residue by column chromatography (silica gel, ethyl acetate/petroleum ether gradient) yields the corresponding lactone.

References


PubMed Literature


Product Documents (Note: Some products will not have analytical charts available.)
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