Basic information Safety Supplier Related

2-AMINOTHIAZOLE-5-CARBONITRILE

Basic information Safety Supplier Related

2-AMINOTHIAZOLE-5-CARBONITRILE Basic information

Product Name:
2-AMINOTHIAZOLE-5-CARBONITRILE
Synonyms:
  • 2-Aminothiazole-5-carbonitrile 97%
  • 2-Amino-1,3-thiazole-5-carbonitrile
  • 2-Amino-1,3-thiazole-5-carbonitrile 97%
  • 2-AMINO-5-CYANOTHIAZOLE
  • 2-AMINOTHIAZOLE-5-CARBONITRILE
  • 2-AMINOTHIAZOLE-5-CARBONITRILE, 95+%
  • 5-thiazolecarbonitrile, 2-amino-
  • 2-amino-1,3-thiazole-5-carbonitrile(SALTDATA: FREE)
CAS:
51640-52-9
MF:
C4H3N3S
MW:
125.15
Product Categories:
  • Amines
  • blocks
  • Carboxes
  • Thiazoles
  • Thiazole
Mol File:
51640-52-9.mol
More
Less

2-AMINOTHIAZOLE-5-CARBONITRILE Chemical Properties

Melting point:
185-187
Boiling point:
330.4±15.0 °C(Predicted)
Density 
1.45±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
form 
solid
pka
1.82±0.10(Predicted)
color 
Dark brown
More
Less

Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-41
Safety Statements 
26-39
RIDADR 
UN3439
WGK Germany 
3
Hazard Note 
Irritant/Keep Cold
HazardClass 
IRRITANT
HazardClass 
6.1
HS Code 
2934100090
More
Less

2-AMINOTHIAZOLE-5-CARBONITRILE Usage And Synthesis

Synthesis

51640-51-8

51640-52-9

5-Cyano-2-trifluoroacetamido thiazole (3.32 g, 15 mmol) was used as raw material, and it was reacted with potassium carbonate (4.0 mL 10% w/v methanol/water (5:2) solution) for 3 hours at 20°C with stirring. After completion of the reaction, the insoluble material was removed by filtration, and the pH of the filtrate was adjusted to 7 with dilute hydrochloric acid and filtered again to remove the insoluble material. Subsequently, the filtrate was evaporated to remove volatiles. The residue was suspended in water and extracted with ethyl acetate. The organic phases were combined, washed sequentially with water and brine, dried over anhydrous magnesium sulfate and evaporated to remove the solvent. The resulting residue was treated with 20% aqueous fluoboric acid (40 mL) and heated at 70 °C for 1 hour. The reaction mixture was cooled, neutralized with solid sodium bicarbonate at 0 °C and extracted with ethyl acetate. The organic phases were combined, dried over anhydrous magnesium sulfate and evaporated to remove volatiles to give 2-amino-5-cyanothiazole (1.79 g, 95% yield) as a final solid product. The product was confirmed by NMR hydrogen spectrum (400.13 MHz): δ 7.83 (1H, s), 8.12 (2H, s); mass spectrum (m/z): 125 [MH]+.

References

[1] Patent: WO2007/31745, 2007, A1. Location in patent: Page/Page column 102-103
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1973, p. 2769 - 2772

2-AMINOTHIAZOLE-5-CARBONITRILESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
PharmaBlock Sciences (Nanjing),Inc.
Tel
025-86918202 4000255188
Email
sales@pharmablock.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18