Basic information Safety Supplier Related

OXAZOLO[4,5-B]PYRIDIN-2(3H)THIONE

Basic information Safety Supplier Related

OXAZOLO[4,5-B]PYRIDIN-2(3H)THIONE Basic information

Product Name:
OXAZOLO[4,5-B]PYRIDIN-2(3H)THIONE
Synonyms:
  • [1,3]Oxazolo[4,5-b]pyridin-2-thiol
  • Oxazolo[4,5-b]pyridine-2(3H)-thione
  • 1,3-Oxazolo[4,5-b]pyridin-2(3H)thione
  • 2,3-Dihydro-2-thioxo-1,3-oxazolo[4,5-b]pyridine
  • Oxazolo[4,5-b]pyridin-2(3H)thione,99%
  • 3H-[1,3]oxazolo[4,5-b]pyridine-2-thione
  • OXAZOLO[4,5-B]PYRIDIN-2(3H)THIONE
  • OXAZOLO[4,5-B]PYRIDINE-2-THIOL
CAS:
53052-06-5
MF:
C6H4N2OS
MW:
152.17
Mol File:
53052-06-5.mol
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OXAZOLO[4,5-B]PYRIDIN-2(3H)THIONE Chemical Properties

Melting point:
243-246 °C
Density 
1.402 (estimate)
refractive index 
1.6430 (estimate)
storage temp. 
2-8°C
form 
solid
Appearance
White to off-white Solid
CAS DataBase Reference
53052-06-5
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Safety Information

Hazard Codes 
Xi
Safety Statements 
24/25
HazardClass 
IRRITANT
HS Code 
2934999090

MSDS

  • Language:English Provider:ACROS
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OXAZOLO[4,5-B]PYRIDIN-2(3H)THIONE Usage And Synthesis

Chemical Properties

Beige crystalline powder

Synthesis

16867-03-1

140-89-6

53052-06-5

Step 1: Synthesis of oxazolo[4,5-b]pyridine-2(3H)thione 2-Amino-3-hydroxypyridine (5.0 g, 45.45 mmol) and potassium ethylxanthate (8.0 g, 49.99 mmol) were dissolved in pyridine (50 mL), and the reaction was stirred at 110 °C overnight. Upon completion of the reaction, the mixture was cooled to 0 °C, ice water was added and acidified with concentrated hydrochloric acid. The precipitated solid was collected by filtration and dried under vacuum to afford the target product oxazolo[4,5-b]pyridine-2(3H)thione (6.0 g, 86.95% yield). Product characterization data: 1H NMR (DMSO-d6, 300 MHz): δ 8.24-8.22 (d, 1H), 7.90-7.87 (d, 1H), 7.30-7.26 (m, 1H). LCMS: m/z 153.0 [M + H]+.

References

[1] Patent: WO2015/104688, 2015, A1. Location in patent: Page/Page column 36
[2] Patent: US2016/340366, 2016, A1. Location in patent: Paragraph 0205; 0206
[3] Monatshefte fur Chemie, 2011, vol. 142, # 9, p. 895 - 899
[4] Journal of Organic Chemistry, 1995, vol. 60, # 17, p. 5721 - 5725
[5] European Journal of Medicinal Chemistry, 2005, vol. 40, # 1, p. 15 - 23

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