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1-ACETYL-3-THIOSEMICARBAZIDE

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1-ACETYL-3-THIOSEMICARBAZIDE Basic information

Product Name:
1-ACETYL-3-THIOSEMICARBAZIDE
Synonyms:
  • ACETYLTHIOSEMICARBAZIDE
  • acetamidothiourea
  • 1-ACETYLTHIOSEMICARBAZIDE
  • 1-ACETYL-3-THIOSEMICARBAZIDE
  • Acetic acid N'-(aminothioxomethyl) hydrazide
  • 1-Acetylthiosemicarbazide,95%
  • 2-acetylhydrazinecarbothioaMide
  • Acetic acid, 2-(aminothioxomethyl)hydrazide
CAS:
2302-88-7
MF:
C3H7N3OS
MW:
133.17
EINECS:
218-956-4
Product Categories:
  • Sulphur Derivatives
Mol File:
2302-88-7.mol
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1-ACETYL-3-THIOSEMICARBAZIDE Chemical Properties

Melting point:
165-170 °C
Density 
1.280 (estimate)
refractive index 
1.7490 (estimate)
storage temp. 
2-8°C(protect from light)
solubility 
DMSO (Sparingly), Methanol (Sparingly)
pka
10.30±0.70(Predicted)
form 
solid
Appearance
Off-white to light yellow Solid
Water Solubility 
Partly soluble in water.
Stability:
Hygroscopic
CAS DataBase Reference
2302-88-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T
Risk Statements 
25-36/37/38
Safety Statements 
24/25-45
RIDADR 
2811
HazardClass 
6.1
PackingGroup 
III
HS Code 
29309099

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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1-ACETYL-3-THIOSEMICARBAZIDE Usage And Synthesis

Chemical Properties

white to slightly beige crystalline powder

Uses

1-Acetyl-3-thiosemicarbazide is applied in pharmaceutical industry as an intermediate.

Synthesis

79-19-6

75-36-5

2302-88-7

General procedure for the synthesis of acetylthiosemicarbazone from aminothiourea and acetyl chloride: preparation of the intermediate 2-acetylcarbazinethioformamide; Acetyl chloride (8.64 g, 0.11 mol) was added slowly and dropwise to an anhydrous tetrahydrofuran (THF, 100 mL) solution of aminothiourea (9.10 g, 0.10 mol) at 0 °C. The reaction mixture was heated to reflux and maintained for 3 hours. Upon completion of the reaction, it was cooled to room temperature and the reaction was quenched by the addition of water (100 mL) followed by extraction with ethyl acetate (3 x 100 mL). The organic phases were combined, washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to remove the solvent. The crude product was purified by column chromatography (eluent: methanol/dichloromethane=1/1, v/v) to afford the target compound acetylthiosemicarbazone (8.64 g, 65% yield). The results of mass spectrometry (electrospray ionization, ESI) analysis: m/z calculated value C3H7N3OS [M+H]+ 133.03, measured value 134.0 (MH+).

References

[1] Patent: WO2009/87220, 2009, A1. Location in patent: Page/Page column 57
[2] Yakugaku Zasshi, 1952, vol. 72, p. 376
[3] Chem.Abstr., 1953, p. 3856
[4] Synthetic Communications, 2004, vol. 34, # 22, p. 4189 - 4198
[5] Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2010, vol. 76, # 5, p. 531 - 536

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