
CAS 24295-03-2: 2-Acetylthiazole
Formula:C5H5NOS
InChI:InChI=1S/C5H5NOS/c1-4(7)5-6-2-3-8-5/h2-3H,1H3
InChI key:InChIKey=MOMFXATYAINJML-UHFFFAOYSA-N
SMILES:C(C)(=O)C1=NC=CS1
Synonyms:- 1-(1,3-Thiazol-2-Yl)Ethanone
- 1-(1,3-Thiazol-2-yl)ethan-1-one
- 1-(2-Thiazolyl)-Ethanone
- 1-(Thiazol-2-yl)ethanone
- 2-Acetyl thiazole
- 2-Acetyl-1,3-thiazole
- 2-Thiazolyl methyl ketone
- Acetylthiazole
- Ethanone, 1-(2-thiazolyl)-
- Ketone, methyl 2-thiazolyl
- Methyl 2-thiazolyl ketone
- See more synonyms
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Found 9 products.
2-Acetylthiazole, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C5H5NOSPurity:99%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:127.162-Acetylthiazole
CAS:2-Acetylthiazole (2-Acetylthiazole;2 Acetylthiazole) is used in the preparation of chiral alcohols, triazolothiazoles, it is also used in aldol condensationFormula:C5H5NOSPurity:98.32%Color and Shape:Clear ColorlessMolecular weight:127.162-Acetylthiazole
CAS:Formula:C5H5NOSPurity:>98.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:127.162-Acetyl-1,3-thiazole
CAS:2-Acetyl-1,3-thiazoleFormula:C5H5NOSPurity:98%Color and Shape: colourless to light yellow liquidMolecular weight:127.16g/mol2-Acetylthiazole
CAS:2-Acetylthiazole is a heterocyclic compound that is a derivative of thiazole. It is used in the production of dyes, pharmaceuticals and other organic compounds. 2-Acetylthiazole can be synthesized by reacting glyoxal with an acid chloride or carboxylic acid to form the corresponding sulfonyl chloride, which can then be reacted with sodium acetate in ethanol to produce 2-acetylthiazole. This reaction was found to proceed efficiently at room temperature and without the need for strong acids or bases. The product has been shown to have anticancer activity in model systems, with carbonyl groups being suggested as a possible mechanism of action. 2-Acetylthiazole is also an intermediate in the synthesis of many other organic compounds and has been shown to react with d-arabinose, producing d-ribofuranose and water.Formula:C5H5NOSPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:127.17 g/mol