Weight | 73.12 g/mol |
---|---|
Formula | C2H3NS |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
METHYL THIOCYANATE (556-64-9)
Score:
#3043 in Chemistry
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- Electron transmission and inner-shell electron energy loss spectroscopy of acetonitrile, isocyanomethane, methyl thiocyanate, and isothiocyanatomethane (The Journal of Physical Chemistry, 1989)
- Quantification of methyl thiocyanate in the headspace of Pseudomonas aeruginosa cultures and in the breath of cystic fibrosis patients by selected ion flow tube mass spectrometry (Rapid Communications in Mass Spectrometry, 2011)
- Synthesis, characterization and demonstration of superoxide dismutase-like activity of copper(II) chloride, bromide, nitrate, thiocyanate, sulphate, and perchlorate complexes with 2-methyl-amino pyridine (Journal of Inorganic Biochemistry, 1996)
- LiquidLiquid Equilibria for the Three Ternary Systems (3-Methyl-N-butylpyridinium Dicyanamide + Toluene + Heptane), (1-Butyl-3-methylimidazolium Dicyanamide + Toluene + Heptane) and (1-Butyl-3-methylimidazolium Thiocyanate + Toluene + Heptane) at T = (313.15 and 348.15) K and p = 0.1 MPa (Journal of Chemical & Engineering Data, 2010)
- Kinetics and mechanism of the reaction of palladium(II) complexes of o-(diphenylphosphino)thioanisole and o-(diphenylphosphino)selenoanisole with nucleophiles thiocyanate and iodide. Carbon-13 NMR spectroscopy of the methyl-heteroatom complexes and x-ray structural characterization of diiodobis(o-(diphenylphosphino)benzenethiolato)dipalladium(II) (Inorganic Chemistry, 1980)
- Allosteric regulation of -amino-3-hydroxy-5-methyl-4-isoxazole-propionate receptors by thiocyanate and cyclothiazide at a common modulatory site distinct from that of 2,3-benzodiazepines (Neuroscience, 1998)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCSC#N
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InChIKeyVYHVQEYOFIYNJP-UHFFFAOYSA-N
- Pubchem - METHYL THIOCYANATE
- Wikipedia - methyl thiocyanate
Methyl thiocyanate is an organic compound with the formula CH3SCN. It is a colourless liquid with an onion-like odor. It is produced by the methylation of thiocyanate salts.
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