2-Cyanothiazole

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Products Intro: Product Name:2-Cyanothiazole
CAS:1452-16-0
Purity:98% Package:25kg
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Products Intro: Product Name:thiazole-2-carbonitrile
CAS:1452-16-0
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Products Intro: Product Name:thiazole-2-carbonitrile
CAS:1452-16-0
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Products Intro: Product Name:2-Cyanothiazole
CAS:1452-16-0
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Company Name: Changzhou Ansciep Chemical Co., Ltd.
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Products Intro: CAS:1452-16-0
Purity:0.99 Package:100g, 500g, 1kg, 25kg, 50kg, 200kg

2-Cyanothiazole manufacturers

  • 2-Cyanothiazole
  • 2-Cyanothiazole pictures
  • $0.00 / 25kg
  • 2024-03-28
  • CAS:1452-16-0
  • Min. Order: 25kg
  • Purity: 98%
  • Supply Ability: Inquiry
  • 2-Cyanothiazole
  • 2-Cyanothiazole pictures
  • $500.00 / 1KG
  • 2019-07-06
  • CAS:1452-16-0
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1ton
2-Cyanothiazole Basic information
Product Name:2-Cyanothiazole
Synonyms:2-Cyanothiazole;2-Thiazolecarbonitrile;Thiazol-2-carbonitril;2-Cyanothiazole thiazole-2-carbonitrile;2-Cyanothiazole,95%;1,3-thiazole-2-carbonitrile cz;Thiazol-2-carbonitrile
CAS:1452-16-0
MF:C4H2N2S
MW:110.14
EINECS:
Product Categories:Clinical hepatitis b&c drug intermediates;cyanide
Mol File:1452-16-0.mol
2-Cyanothiazole Structure
2-Cyanothiazole Chemical Properties
Boiling point 203℃
density 1.33
Fp 76℃
storage temp. 2-8°C
form Solid
pka-1.13±0.10(Predicted)
AppearanceLight brown to brown Oil
Water Solubility Slightly soluble in water.
InChIInChI=1S/C4H2N2S/c5-3-4-6-1-2-7-4/h1-2H
InChIKeyZIRGWUZHKJDYKT-UHFFFAOYSA-N
SMILESS1C=CN=C1C#N
CAS DataBase Reference1452-16-0
Safety Information
RIDADR 3439
HazardClass 6.1
PackingGroup 
HS Code 2934100090
MSDS Information
2-Cyanothiazole Usage And Synthesis
Uses2-Cyanothiazole is used as a intermediate for pharmaceutical and chemical research.
Synthesis
1,3-Thiazole-2-carbaldehyde

10200-59-6

2-Cyanothiazole

1452-16-0

GENERAL METHOD: 2-formylthiazole (54 mg, 0.5 mmol) and ammonium acetate (385 mg, 5.0 mmol) were dissolved in acetonitrile (6 mL) at room temperature, followed by the addition of trimethylphenyltrimethylammonium (376 mg, 1.0 mmol). The reaction mixture was stirred at room temperature for 21 h. The reaction mixture was sequentially treated with 0.5 M Na2S2O3 aqueous solution (10 mL) and 1.0 M NaHCO3 aqueous solution (15 mL), and then extracted with ethyl acetate (60 mL). The organic layer was washed sequentially with 0.5 M Na2S2O3 aqueous solution and saturated NaCl aqueous solution, and finally dried with anhydrous MgSO4.

References[1] Heterocycles, 2016, vol. 92, # 10, p. 1796 - 1802
[2] Patent: EP1555257, 2005, A1. Location in patent: Page/Page column 25
[3] Tetrahedron Letters, 2013, vol. 54, # 17, p. 2177 - 2179
[4] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 3, p. 496 - 500
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