CAS 4274-15-1
:Tetraethylthiourea
Description:
Tetraethylthiourea (TETU) is an organic compound characterized by its structure, which features a thiourea backbone with four ethyl groups attached to the nitrogen atoms. It is typically a colorless to pale yellow liquid with a distinctive odor. TETU is known for its role as a reagent in organic synthesis and as a ligand in coordination chemistry. It exhibits solubility in polar organic solvents and has a relatively low boiling point. The compound is of interest due to its ability to form complexes with various metal ions, making it useful in catalysis and extraction processes. However, tetraethylthiourea is also recognized for its potential toxicity and environmental hazards, necessitating careful handling and disposal. Its chemical properties include the ability to participate in nucleophilic reactions, and it can act as a source of thiol groups in various chemical transformations. As with many thiourea derivatives, TETU may exhibit biological activity, warranting further investigation into its effects and applications in medicinal chemistry.
Formula:C9H20N2S
InChI:InChI=1S/C9H20N2S/c1-5-10(6-2)9(12)11(7-3)8-4/h5-8H2,1-4H3
InChI key:InChIKey=ZSPQVOFATJEJMT-UHFFFAOYSA-N
SMILES:C(N(CC)CC)(N(CC)CC)=S
Synonyms:- N,N,N′,N′-Tetraethylthiourea
- Tetraethylthiourea
- Thiourea, tetraethyl-
- Urea, 1,1,3,3-tetraethyl-2-thio-
- thiourea, N,N,N',N'-tetraethyl-
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Found 4 products.
Tetraethylthiourea
CAS:Controlled Product<p>Applications Tetraethylthiourea is an impurity of Disulfiram (D493640) which is used as rubber accelerator; vulcanizer; seed disinfectant; fungicide; alcohol deterrent.<br>References Child, C., et al.: Acta Pharmacol. Toxicol., 8, 305 (1952), Nash, N.G., et al.: Anal. Profiles Drug Subs., 4, 168 (1975),<br></p>Formula:C9H20N2SColor and Shape:NeatMolecular weight:188.33Tetraethylthiourea-d10
CAS:Controlled ProductFormula:C9D10H10N2SColor and Shape:NeatMolecular weight:198.395


