| Weight | 99.158 g/mol |
|---|---|
| Formula | C4H5NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Methylthiazole (3581-87-1)
Score:
#64 in Medicinal chemistry
,
#7224 in Chemistry
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- Activity of rat cytosolic thioredoxin reductase is strongly decreased by trans-[bis(2-amino-5- methylthiazole)tetrachlororuthenate(III)]: first report of relevant thioredoxin reductase inhibition for a ruthenium compound. (Journal of Medicinal Chemistry, 2007)
- Electrochemical oxidation of substituted thiazoles: 2-amino-4-ethoxycarbonyl-5- methylthiazole and N-ethoxycarbonyl-N- (4-ethoxycarbonyl-5-methylthiazol-2-yl) thiourea (Electrochimica Acta, 1979)
- Derivatives of 2-Amino-4-methylthiazole (Journal of the American Chemical Society, 1946)
- Synthesis and pharmacological evaluation of a novel series of 3-aryl-2-(2-substituted-4-methylthiazole-5-yl)thiazolidin-4-one as possible anti-inflammatory and antimicrobial agents (Bioorganic & Medicinal Chemistry Letters, 2012)
- Thiamin analogs. 2. 4-Methylthiazole analogs. (Journal of the American Chemical Society, 1945)
- Palladium-catalyzed cross-coupling reaction of 4-methylthiazole and 2-trimethylsilylthiazoles with biaryl triflates (Heterocycles, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=NC=CS1
-
InChIKeyVZWOXDYRBDIHMA-UHFFFAOYSA-N
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