| Weight | 45.041 g/mol |
|---|---|
| Formula | CH3NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
formamide (75-12-7)
Score:
#524 in Physics
,
#1522 in Chemistry
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- Sigma-Aldrich - Search for formamide
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- Determining atom-centered monopoles from molecular electrostatic potentials. The need for high sampling density in formamide conformational analysis (Journal of Computational Chemistry, 1990)
- Rates of formation and thermal stabilities of RNA:DNA and DNA:DNA duplexes at high concentrations of formamide (Nucleic Acids Research, 1977)
- Nucleic acid reassociation in formamide. (Biochemistry, 1969)
- Solvent effects. 3. Tautomeric equilibria of formamide and 2-pyridone in the gas phase and solution: an ab initio SCRF study (Journal of the American Chemical Society, 1992)
- Microwave Spectrum and Molecular Structure of Formamide (Journal of Chemical Physics, 1960)
- Determination of partial atomic charges from ab initio molecular electrostatic potentials. Application to formamide, methanol, and formic acid (The Journal of Physical Chemistry, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B - H360: May damage fertility or the unborn child
Danger Reproductive toxicity - Category 1A, 1B -
SMILESC(=O)N
-
InChIKeyZHNUHDYFZUAESO-UHFFFAOYSA-N
- Pubchem - formamide
- Wikipedia - formamide
Formamide, also known as methanamide, is an amide derived from formic acid. It is a clear liquid which is miscible with water and has an ammonia-like odor. It is chemical feedstock for the manufacture of sulfa drugs, other pharmaceuticals, herbicides, pesticides and the manufacture of hydrocyanic acid.
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formamide
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