| Weight | 42.017 g/mol |
|---|---|
| Formula | CNO- |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
cyanate (661-20-1, 71000-82-3)
Score:
#1271 in Physics
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#2938 in Biology
,
#3679 in Chemistry
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- Reactions of the Cyanate Present in Aqueous Urea with Amino Acids and Proteins (Journal of Biological Chemistry, 1960)
- Chemistry and Technology of Cyanate Ester Resins (1994)
- The Use of Cyanate for the Determination of NH2-terminal Residues in Proteins (Journal of Biological Chemistry, 1963)
- Reactions of Cyanate with Functional Groups of Proteins. III. Reactions with Amino and Carboxyl Groups (Biochemistry, 1965)
- Cyanate Ester Resins, Recent Developments (Advances in Polymer Science, 2001)
- Potassium Cyanate as an Inhibitor of the Sickling of Erythrocytes In Vitro (Proceedings of the National Academy of Sciences of the United States of America, 1971)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESC(#N)[O-]
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InChIKeyXLJMAIOERFSOGZ-UHFFFAOYSA-M
- Pubchem - cyanate
- Wikipedia - cyanate ion
The cyanate ion is an anion with the chemical formula written as [OCN] or [NCO]. In aqueous solution it acts as a base, forming isocyanic acid, HNCO. The cyanate ion is an ambidentate ligand, forming complexes with a metal ion in which either the nitrogen or oxygen atom may be the electron-pair donor.
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