Oxazole-2-amine

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Company Name: Tianjin Yao Technology Development Co., Ltd.  Gold
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Company Name: goldenchemical  Gold
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Company Name: SelectLab Chemicals GmbH  
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Oxazole-2-amine manufacturers

  • Oxazole-2-amine
  • Oxazole-2-amine pictures
  • $780.00
  • 2024-02-23
  • CAS:4570-45-0
  • Min. Order: 1g
  • Purity: 97
  • Supply Ability: 500 Kg
  • Oxazole-2-amine
  • Oxazole-2-amine pictures
  • $15.00
  • 2021-07-13
  • CAS:4570-45-0
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Oxazole-2-amine
  • Oxazole-2-amine pictures
  • $15.00
  • 2021-07-10
  • CAS:4570-45-0
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
Oxazole-2-amine Basic information
Product Name:Oxazole-2-amine
Synonyms:2-Amino-1,3-oxazole;OXAZOLE-2-YLAMINE;Oxazole-2-amine;OXAZOL-2-YLAMINE;2-Amino Oxazole Or 1,3-Oxazol-2-amine;2-OxazolaMine;2,3-dihydro-1,3-oxazol-2-amine;2-Aminooxazole >
CAS:4570-45-0
MF:C3H4N2O
MW:84.08
EINECS:
Product Categories:Amines;Oxazoles, Isoxazoles & Benzoxazoles;Naphthyridine,Quinoline;Oxazoles, Isoxazoles & Benzoxazoles;Building Blocks;Oxazole
Mol File:4570-45-0.mol
Oxazole-2-amine Structure
Oxazole-2-amine Chemical Properties
Melting point 93-95℃
Boiling point 186.7±23.0 °C(Predicted)
density 1.241±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO (Soluble), Ethyl Acetate (Slightly)
form Solid
pka5.45±0.10(Predicted)
color Off-White to Pale Yellow
λmax219nm(MeOH)(lit.)
InChIInChI=1S/C3H4N2O/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)
InChIKeyACTKAGSPIFDCMF-UHFFFAOYSA-N
SMILESO1C=CN=C1N
CAS DataBase Reference4570-45-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 34-36/37/38
Safety Statements 26-36/37/39-45-24/25
RIDADR 2735
WGK Germany 3
HazardClass IRRITANT
HS Code 29349990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
Oxazole-2-amine Usage And Synthesis
Uses2-Aminooxazole is a chemical reagent used in the synthesis of novel inhibitors of the kinetoplastid Trypanosoma brucei.
Synthesis
Cyanamide

420-04-2

GLYCOLALDEHYDE

141-46-8

Oxazole-2-amine

4570-45-0

Example 2: Preparation of 2-aminooxazole. To a tetrahydrofuran (THF, 60 mL) solution of cyanamide (19.8 mL, 50% w/w aqueous solution, 0.25 mol) was added a 24 mL aqueous solution of 2-hydroxyacetaldehyde (15 g, 0.25 mol). The reaction mixture was treated with 2 M aqueous sodium hydroxide (25.2 mL, 0.05 mol) at 0 °C. The mixture was slowly warmed to room temperature and stirred continuously for 24 hours. Upon completion of the reaction, the volatile solvent (THF) was removed by distillation under reduced pressure. The remaining aqueous solution was extracted with ethyl acetate (4 × 200 mL). The organic phases were combined, dried with anhydrous sodium sulfate, and subsequently concentrated under reduced pressure to give 14.968 g (71.3% yield) of white solid product. The product was characterized by 400 MHz 1H NMR (CDCl3): δ 7.13 (s, 1H), 6.74 (s, 1H), 5.26 (br.s, 2H). Elemental analysis calculated values (C3H4N2O): C 42.86%, H 4.80%, N 33.32%; measured values: C 43.01%, H 4.87%, N 33.11%.

References[1] Patent: WO2007/123892, 2007, A2. Location in patent: Page/Page column 50
[2] Patent: WO2004/110990, 2004, A2. Location in patent: Page 37
[3] Patent: WO2006/44869, 2006, A1. Location in patent: Page/Page column 132
[4] Chemistry - A European Journal, 2013, vol. 19, # 14, p. 4586 - 4595
[5] Synthesis, 1976, p. 591 - 593
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