CAS 656-32-6
:N-(2-Fluorophenyl)thiourea
Description:
N-(2-Fluorophenyl)thiourea is an organic compound characterized by the presence of a thiourea functional group attached to a 2-fluorophenyl moiety. Its molecular structure features a thiourea group (-NH-C(=S)-NH-) linked to a phenyl ring that has a fluorine atom substituted at the ortho position. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of thioureas, including the ability to participate in various chemical reactions, such as nucleophilic substitutions and condensation reactions. N-(2-Fluorophenyl)thiourea may also exhibit biological activity, making it of interest in pharmaceutical research. Its CAS number, 656-32-6, allows for easy identification in chemical databases. As with many thioureas, it is important to handle this compound with care due to potential toxicity and environmental concerns. Proper safety measures should be observed when working with this substance in laboratory settings.
Formula:C7H7FN2S
InChI:InChI=1S/C7H7FN2S/c8-5-3-1-2-4-6(5)10-7(9)11/h1-4H,(H3,9,10,11)
InChI key:InChIKey=WYVZQQOFMQRNPF-UHFFFAOYSA-N
SMILES:N(C(N)=S)C1=C(F)C=CC=C1
Synonyms:- (2-Fluorophenyl)thiourea
- 1-(2-Fluorophenyl)Thiourea
- 2-Fluorophenylthiourea
- N-(2-Fluorophenyl)thiourea
- Thiourea, (2-fluorophenyl)-
- Thiourea, N-(2-fluorophenyl)-
- Urea, 1-(o-fluorophenyl)-2-thio-
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Found 5 products.
1-(2-Fluorophenyl)thiourea
CAS:Formula:C7H7FN2SPurity:97%Color and Shape:SolidMolecular weight:170.20731-(2-Fluorophenyl)-2-thiourea
CAS:<p>1-(2-Fluorophenyl)-2-thiourea</p>Formula:C7H7FN2SPurity:97%Color and Shape: white to off white solidMolecular weight:170.21g/mol(2-Fluorophenyl)thiourea
CAS:Formula:C7H7FN2SPurity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:170.211-(2-Fluorophenyl)-2-thiourea
CAS:Formula:C7H7FN2SPurity:97%Color and Shape:SolidMolecular weight:170.21N-(2-Fluorophenyl)thiourea
CAS:<p>N-(2-Fluorophenyl)thiourea is a ligand that interacts with the γ-aminobutyric acid receptor protein. It is synthesized by reacting an amine with thiourea in the presence of acetic acid. The N-(2-Fluorophenyl)thiourea was found to be toxic to rats and mice, but not rabbits or dogs. The toxicity may be due to its ability to form hydrogen bonds with other molecules.</p>Formula:C7H7FN2SPurity:Min. 95%Molecular weight:170.21 g/mol




