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2-PROPIONYLTHIAZOLE

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2-PROPIONYLTHIAZOLE Basic information

Product Name:
2-PROPIONYLTHIAZOLE
Synonyms:
  • 1-(2-thiazolyl)-1-propanon
  • 2-propionylthiazol
  • 2-propionyl-thiazol
  • 2-thiazolyl-1-propanone
  • Thiazole, 2-(1-oxopropyl)
  • Thiazole, 2-propionyl-
  • ETHYL 2-THIAZOLYL KETONE
  • FEMA NUMBER 3611
CAS:
43039-98-1
MF:
C6H7NOS
MW:
141.19
Product Categories:
  • thiazole Flavor
Mol File:
43039-98-1.mol
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2-PROPIONYLTHIAZOLE Chemical Properties

Boiling point:
110°C/5mm
Density 
1.174
refractive index 
1.5350-1.5390
FEMA 
3611 | 2-PROPIONYLTHIAZOLE
Flash point:
110°C/5mm
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
pka
-0.03±0.10(Predicted)
color 
Colorless to Light yellow to Light orange
Odor
at 0.10 % in dipropylene glycol. cereal bread nutty popcorn
Odor Type
bready
Water Solubility 
Not miscible or difficult to mix with water.
JECFA Number
1042
LogP
0.90
CAS DataBase Reference
43039-98-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
10-36/37/38-41-37/38-22
Safety Statements 
26-36/37/39-39
RIDADR 
1993
RTECS 
XJ5123000
HazardClass 
IRRITANT
HS Code 
2934100090

MSDS

  • Language:English Provider:ALFA
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2-PROPIONYLTHIAZOLE Usage And Synthesis

Occurrence

Reported found in lard.

Uses

Used as flavoring agent and fragrance chemical compounds.

Synthesis

112969-95-6

43039-98-1

GENERAL PROCEDURE: A flame-dried and cooled round-bottomed flask under nitrogen protection was charged with allyl alcohol 51 (0.5 mmol) and tetrahydrofuran (THF, 2.5 mL). The reaction mixture was stirred at 0 °C for 5 min before a one-time addition of sodium hydride (NaH, 1 mmol, 2 equiv.), followed by a slow warming of the mixture to room temperature. Upon completion of the reaction, the reaction was quenched by the addition of saturated ammonium chloride (NH4Cl, 2 mL). The reaction mixture was extracted with ethyl acetate (EtOAc, 10 mL × 2) and the combined organic phases were washed with saturated saline (15 mL). The organic layer was dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure to remove the solvent, and the residue was purified by silica gel column chromatography to give the target ketone product 52.

References

[1] Tetrahedron, 2011, vol. 67, # 19, p. 3406 - 3411

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