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CAS RN: 4568-71-2 | Product Number: B1224

3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium Chloride

Chemical Structure of 3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium Chloride

Purity: >98.0%(T)(HPLC)
Synonyms:
Product Documents:
25G
₹5,300.00
3   22  

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Product Number B1224
Purity / Analysis Method >98.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__1__3H__1__6ClNOS = 269.79 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Hygroscopic
CAS RN 4568-71-2
Reaxys Registry Number 3788921
PubChem Substance ID 87564160
SDBS (AIST Spectral DB) 18321
MDL Number

MFCD00011959

Specifications
Appearance White to Light yellow powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Nonaqueous Titration) min. 98.0 %
Melting point 142.0 to 145.0 °C
NMR confirm to structure
Properties (reference)
Melting Point 143 °C
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
Related Laws:
Transport Information:
Application
Acyloin Condensation of Aliphatic Aldehydes Using Thiazolinium Ion Catalyst

Typical procedure:
A 500 mL, three-necked round-bottomed flask is charged with 3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium Chloride (13.4 g, 0.05 mol), butyraldehyde (72.1 g, 1.0 mol), triethylamine (30.3 g, 0.3 mol), and absolute ethanol (300 mL). The mixture is stirred and heated at 80°C. After 1.5 h the reaction mixture is cooled to room temperature and concentrated by rotary evaporation. The residual yellow liquid is poured into 500 mL of water and extracted with 150 mL of dichloromethane. The aqueous layer is extracted with a second 150 mL portion of dichloromethane. The combined organic phases are washed with 300 mL of saturated sodium bicarbonate and with 300 mL of water. The dichloromethane is removed by rotary evaporation. Distillation through a 20 cm Vigreux column gives 51–54 g (71–74%) of product as a colorless to light-yellow liquid.

References


Application
Useful N-Heterocyclic Carbene Precursor for Diastereoselective Cyclization Reaction

References


PubMed Literature


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