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1-Propanesulfonyl chloride

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1-Propanesulfonyl chloride Basic information

Product Name:
1-Propanesulfonyl chloride
Synonyms:
  • 1-PROPANESULFONYL CHLORIDE
  • PROPANE-1-SULFONYL CHLORIDE
  • PROPANE SULFONYL CHLORIDE
  • 1-Propanesulfonyl Chloride, Pract.
  • Propane-1-sulphonyl chloride 97%
  • propanesulphonyl chloride
  • Propane-1-sulfonic acid chloride
  • 1-Propanesulfonyl chloride,99%
CAS:
10147-36-1
MF:
C3H7ClO2S
MW:
142.6
EINECS:
233-414-7
Product Categories:
  • Organic Building Blocks
  • Sulfonyl Halides
  • Sulfur Compounds
  • Agrochemical Intermediates
Mol File:
10147-36-1.mol
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1-Propanesulfonyl chloride Chemical Properties

Melting point:
-37 °C
Boiling point:
78-79 °C/15 mmHg (lit.)
Density 
1.267 g/mL at 25 °C (lit.)
vapor density 
4.9 (vs air)
refractive index 
n20/D 1.453(lit.)
Flash point:
176 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
clear liquid
color 
Colorless to Light yellow
Water Solubility 
Decomposes in hot water.
Sensitive 
Moisture Sensitive
BRN 
1747500
CAS DataBase Reference
10147-36-1(CAS DataBase Reference)
NIST Chemistry Reference
1-Propanesulfonyl chloride(10147-36-1)
EPA Substance Registry System
1-Propanesulfonyl chloride (10147-36-1)
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Safety Information

Hazard Codes 
C
Risk Statements 
14-34-36-R36-R34-R14
Safety Statements 
26-36/37/39-45-S45-S36/37/39-S26
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
10-19-21
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29049090

MSDS

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1-Propanesulfonyl chloride Usage And Synthesis

Chemical Properties

Light yellow liquid

Uses

1-Propanesulfonyl chloride was used in synthesis of 1-alkyl-3-methylimidazolium alkanesulfonate ionic liquids.

Synthesis

2,4,6-Trichloro-[1,3,5]-triazine (TCT) was added at room temperature to a solution of propane-1-sulfonic acid in acetone dry, followed by NEt3 dropwise. The resulting mixture was irradiated to 80 °C (50 W of MW power) for 20 min in a sealed tube (10 mL pressure-rated reaction vial) in a self-tuning single-mode irradiating synthesizer. The mixture was cooled rapidly to room temperature by passing compressed air through the microwave cavity for 1 min. After cooling to room temperature, the precipitate was filtered off on Celite to afford 1-Propanesulfonyl chloride[1].

References

[1] Lidia De Luca, Giampaolo Giacomelli. “An Easy Microwave-Assisted Synthesis of Sulfonamides Directly from Sulfonic Acids.” The Journal of Organic Chemistry 73 10 (2008): 3967–3969.

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