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2-[(Acetylthio)methyl]-phenylpropionic acid

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2-[(Acetylthio)methyl]-phenylpropionic acid Basic information

Product Name:
2-[(Acetylthio)methyl]-phenylpropionic acid
Synonyms:
  • 2-[(Acetylthio)methyl]-phenylpropionic acid
  • 2-[(ACETYLETHIO)METHYL]PHENYLPROPIONIC ACID
  • 2-[(Acetylthio)methyl]-3-phenylpropanoic acid 96%
  • 3-(Acetylsulphanyl)-2-benzylpropanoic acid
  • α-[(Acetylthio)Methyl]benzenepropanoic Acid
  • 2-[(ACETYLTHIO)METHYL]-3-PHENYLPROPIONIC ACIDE
  • 2-(Acetylthiomethyl)-3-phenylpropionic Acid
  • 2-[(Acetylsulfanyl)methyl]-3-phenylpropionic Acid
CAS:
91702-98-6
MF:
C12H14O3S
MW:
238.3
Product Categories:
  • Aromatics
  • Intermediates
  • Sulfur & Selenium Compounds
  • (intermediate of racecodotril)
Mol File:
91702-98-6.mol
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2-[(Acetylthio)methyl]-phenylpropionic acid Chemical Properties

Melting point:
39 °C
Boiling point:
381.9±35.0 °C(Predicted)
Density 
1.226±0.06 g/cm3(Predicted)
refractive index 
1.55
storage temp. 
2-8°C(protect from light)
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
powder to lump to clear liquid
pka
4.06±0.10(Predicted)
color 
White or Colorless to Yellow
CAS DataBase Reference
91702-98-6
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Safety Information

HS Code 
2930909899
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2-[(Acetylthio)methyl]-phenylpropionic acid Usage And Synthesis

Chemical Properties

Brownish Liquid

Uses

2-[(Acetylthio)methyl]-phenylpropionic acid is a racecadotril intermediate. It is also a β-thiopropionyl-amino acid derivative used as β-lactamase inhibitor.

Synthesis

5669-19-2

507-09-5

91702-98-6

General procedure for the synthesis of 3-(acetylthio)-2-benzylpropionic acid from 2-benzylpropenoic acid and thioacetic acid: 16.2 g of 2-benzylpropenoic acid and 12.3 mL of thioacetic acid were added to a clean and dry round-bottomed flask, and the reaction was stirred for 1 hour at 30 °C. Subsequently, the reaction mixture was warmed up to 60 °C and the stirring reaction was continued for 4 hours. Upon completion of the reaction, the excess thioacetic acid was removed by distillation to give the crude product of 3-(acetylthio)-2-benzylpropionic acid. Yield: 23.8 g.

References

[1] Journal of Medicinal Chemistry, 1994, vol. 37, # 15, p. 2461 - 2476
[2] Journal of Organic Chemistry, 2009, vol. 74, # 9, p. 3389 - 3393
[3] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 20, p. 5614 - 5619
[4] Journal of Medicinal Chemistry, 1992, vol. 35, # 3, p. 602 - 608
[5] Magnetic Resonance in Chemistry, 2000, vol. 38, # 6, p. 468 - 471

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