Weight | 76.124 g/mol |
---|---|
Formula | CH4N2S |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Thiourea (62-56-6)
Score:
#111 in Physics
,
#278 in Biology
,
#288 in Chemistry
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- Enantio- and diastereoselective Michael reaction of 1,3-dicarbonyl compounds to nitroolefins catalyzed by a bifunctional thiourea. (Journal of the American Chemical Society, 2005)
- Urea and ThioureaSubstituted Cinchona Alkaloid Derivatives as Highly Efficient Bifunctional Organocatalysts for the Asymmetric Addition of Malonate to Nitroalkenes: Inversion of Configuration at C9 Dramatically Improves Catalyst Performance. (Angewandte Chemie, 2005)
- CimetidineA Non-Thiourea H2-Receptor Antagonist (Journal of International Medical Research, 1975)
- Anion complexation and sensing using modified urea and thiourea-based receptors (Chemical Society Reviews, 2010)
- Efficient and Simple Colorimetric Fluoride Ion Sensor Based on Receptors Having Urea and Thiourea Binding Sites (Organic Letters, 2004)
- Highly enantioselective direct conjugate addition of ketones to nitroalkenes promoted by a chiral primary amine-thiourea catalyst. (Journal of the American Chemical Society, 2006)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B - H351: Suspected of causing cancer
Warning Carcinogenicity - Category 2 - H361: Suspected of damaging fertility or the unborn child
Warning Reproductive toxicity - Category 2 - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 -
SMILESC(=S)(N)N
-
InChIKeyUMGDCJDMYOKAJW-UHFFFAOYSA-N
- Pubchem - Thiourea
- Wikipedia - thiourea
Thiourea () is an organosulfur compound with the formula SC(NH2)2 . It is structurally similar to urea, except that the oxygen atom is replaced by a sulfur atom, but the properties of urea and thiourea differ significantly. Thiourea is a reagent in organic synthesis.
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Alternate Names
Estimated Properties
Boiling Point | 277.57 C | EPA T.E.S.T. |
---|---|---|
Density | 1.18 g/cm3 | EPA T.E.S.T. |
Flash Point | 62.78 C | EPA T.E.S.T. |
Water Solubility | 97127.4 mg/L | EPA T.E.S.T. |
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