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CAS RN: 26412-87-3 | Product Number: P0998

Pyridine - Sulfur Trioxide Complex


Purity: >95.0%(T)
Synonyms:
  • Sulfur Trioxide - Pyridine Complex
Product Documents:
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Product Number P0998
Purity / Analysis Method >95.0%(T)
Molecular Formula / Molecular Weight C__5H__5N·SO__3 = 159.16 
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 Moisture Sensitive
CAS RN 26412-87-3
Reaxys Registry Number 3704116
PubChem Substance ID 87575111
MDL Number

MFCD00012437

Specifications
Appearance White to Light yellow powder to crystal
Purity(Ethanolysis Method) min. 95.0 %
NMR confirm to structure
Properties (reference)
GHS
Pictogram Pictogram Pictogram
Signal Word Danger
Hazard Statements H302 : Harmful if swallowed.
H314 : Causes severe skin burns and eye damage.
H290 : May be corrosive to metals.
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 247-683-3
Transport Information:
UN Number UN3261
Class 8
Packing Group III
HS Number 2933310000
Application
TCI Practical Example: Synthesis of the Aldehyde Utilizing the Parikh-Doering Oxidation

Parikh-Doering酸化によるアルデヒドの合成

Used Chemicals

Procedure

To a solution of 3,5-dibenzyloxybenzyl alcohol (1.0 g, 3.1 mmol), N,N-diisopropylethylamine (2.7 mL, 15.6 mmol, 5.0 equiv), and DMSO (2.22 mL, 31 mmol, 10 equiv) in dichloromethane (10 mL) was added SO3·Py (1.49 g, 9.4 mmol, 3.0 equiv) at 0 °C. The reaction mixture was stirred at same temperature for 1 hour and quenched with Na2S2O3 aq. (20 mL) was added to the reaction mixture. The aqueous layer was extracted with dichloromethane (20 mL) and washed brine. The organic phase was concentrated under reduced pressure and the residue was purified by column chromatography (ethyl acetate:hexane = 0:1 - 1:1 on silica gel) to give 3,5-dibenzyloxybenzaldehyde as a white solid (850 mg,y. 85%).

Experimenter’s Comments

The reaction mixture was monitored by LC.
This reaction produces dimethyl sulfide, which gives off a bad smell. So that it is recommended to treat this reaction in a fume hood.

Analytical Data

3,5-dibenzyloxybenzaldehyde

1H NMR (270 MHz, CDCl3); δ 9.90 (s, 1H), 7.45-7.32 (m, 10H), 7.12 (d, J = 2.1 Hz, 2H), 6.87 (t, 1H, J = 2.1 Hz), 5.93 (s, 4H).

Lead Reference

Other References


Application
with DMSO or LiAlH4

References


PubMed Literature


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