CAS 2454-39-9
:2-Aminobenzenecarbothioamide
Description:
2-Aminobenzenecarbothioamide, also known as thiourea derivative, is an organic compound characterized by the presence of an amino group and a thiocarbonyl functional group attached to a benzene ring. Its molecular structure features a benzene ring substituted with an amine (-NH2) and a thiocarbonamide (-C(S)NH2) group, which contributes to its reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit properties such as solubility in polar solvents, depending on the specific conditions. 2-Aminobenzenecarbothioamide can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it of interest in synthetic organic chemistry. Additionally, it may have applications in pharmaceuticals and agrochemicals due to its potential biological activities. Safety data should be consulted for handling, as with many chemical substances, it may pose health risks if not managed properly.
Formula:C7H8N2S
InChI:InChI=1S/C7H8N2S/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H2,9,10)
InChI key:InChIKey=HPZKAJRFABCGFF-UHFFFAOYSA-N
SMILES:C(N)(=S)C1=C(N)C=CC=C1
Synonyms:- 2-Aminobenzene-1-carbothioamide
- 2-Aminobenzenecarbothioamide
- 2-Aminobenzenethioamide
- 2-Aminobenzothioamide
- Benzamide, o-aminothio-
- Benzenecarbothioamide, 2-amino-
- Thioanthranilamide
- o-Aminothiobenzamide
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
2-Aminothiobenzamide, 97%
CAS:<p>It can be heated to produce 2-trifluoromethyl-3H-quinazoline-4-thione in the presence of reagent molecular sieves and solvent CHCl3 with reaction time of 2 hours. It is an important organic intermediate used in agrochemicals, pharmaceuticals and dyestuff fields. This Thermo Scientific Chemicals bran</p>Formula:C7H8N2SPurity:97%Molecular weight:152.21Benzenecarbothioamide, 2-amino-
CAS:Formula:C7H8N2SPurity:97%Color and Shape:SolidMolecular weight:152.2168
