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CAS RN: 63212-53-3 | Product Number: C0905

2-Chloro-3-ethylbenzoxazolium Tetrafluoroborate


Purity: >97.0%(T)(N)
Synonyms:
Product Documents:
5G
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25G
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Product Number C0905
Purity / Analysis Method >97.0%(T)(N)
Molecular Formula / Molecular Weight C__9H__9BClF__4NO = 269.43 
Physical State (20 deg.C) Solid
Storage Temperature Frozen (<0°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Moisture Sensitive,Heat Sensitive
CAS RN 63212-53-3
Reaxys Registry Number 19236082
PubChem Substance ID 87565961
SDBS (AIST Spectral DB) 11266
MDL Number

MFCD00011943

Specifications
Appearance White to Almost white powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(with Total Nitrogen) min. 97.0 %
Purity(Argentometric Titration) min. 97.0 %
NMR confirm to structure
Properties (reference)
Melting Point 131 °C
GHS
Pictogram Pictogram Pictogram
Signal Word Danger
Hazard Statements H302 : Harmful if swallowed.
H314 : Causes severe skin burns and eye damage.
Precautionary Statements P260 : Do not breathe dust.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water.
P301 + P330 + P331 : IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P304 + P340 + P310 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/doctor.
P305 + P351 + P338 + P310 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/doctor.
Related Laws:
EC Number 263-998-9
Transport Information:
UN Number UN1759
Class 8
Packing Group III
HS Number 2934999090
Application
Activating Agent for Hydroxy Groups

Experimental procedure: To a stirred suspension of 2-chloro-3-ethylbenzoxazolium tetrafluoroborate (1.3 mmol) and tetraethylammonium chloride (1.0 mmol) in dichloromethane (2 mL) cooled to 0 °C is added triethylamine (1.3 mmol) in dichloromethane (1 mL) under an argon atmosphere. To the yellow suspension is added dropwise 3β-cholestanol (1.0 mmol) in dichloromethane (1.5 mL) and the resulting mixture is stirred at the same temperature for additional 4 h. After evaporation of the solvent reduced pressure, the residue is directly chromatographed on silica gel eluting with hexane to give 1 in 85% yield.

References


PubMed Literature


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