CAS 55489-15-1
:5-Ethoxy-2-mercaptobenzimidazole
Description:
5-Ethoxy-2-mercaptobenzimidazole is an organic compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. The presence of an ethoxy group at the 5-position and a mercapto group (-SH) at the 2-position contributes to its unique chemical properties. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents, while its solubility in water may vary. The mercapto group imparts thiol characteristics, making it reactive towards electrophiles and capable of forming disulfide bonds. Additionally, the ethoxy group enhances its lipophilicity, potentially influencing its biological activity and interactions. 5-Ethoxy-2-mercaptobenzimidazole may exhibit antioxidant properties and has been studied for its potential applications in pharmaceuticals, particularly in the development of drugs targeting various biological pathways. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.
Formula:C9H10N2OS
InChI:InChI=1S/C9H10N2OS/c1-2-12-6-3-4-7-8(5-6)11-9(13)10-7/h3-5H,2H2,1H3,(H2,10,11,13)
InChI key:InChIKey=WUSCBOFBIYZVCQ-UHFFFAOYSA-N
SMILES:S=C1NC=2C(=CC(OCC)=CC2)N1
Synonyms:- 2-Mercapto-5-ethoxybenzimidazole
- 2H-Benzimidazole-2-thione, 5-ethoxy-1,3-dihydro-
- 5-Ethoxy-1H-benzimidazole-2-thiol
- 5-Ethoxybenzimidazole-2-thiol
- 5-ethoxy-1,3-dihydro-2H-benzimidazole-2-thione
- 5-Ethoxy-2-mercaptobenzimidazole
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Found 6 products.
5-Ethoxy-1H-benzo[d]imidazole-2-thiol
CAS:Formula:C9H10N2OSPurity:98%Color and Shape:SolidMolecular weight:194.25355-Ethoxy-2-mercaptobenzimidazole
CAS:5-Ethoxy-2-mercaptobenzimidazolePurity:99%Molecular weight:194.25g/mol5-Ethoxy-1H-benzo[d]imidazole-2-thiol
CAS:Formula:C9H10N2OSPurity:95%Color and Shape:Crystalline PowderMolecular weight:194.255-Ethoxy-2-mercaptobenzimidazole
CAS:<p>5-Ethoxy-2-mercaptobenzimidazole is a corrosion inhibitor that has been shown to inhibit the growth of cancer cells by causing them to undergo apoptotic cell death. It also has a protective effect on nerve cells, as evidenced by its ability to prevent the neurotoxic effects of hydrochloric acid. 5-Ethoxy-2-mercaptobenzimidazole is synthesized from 2-(2'-hydroxyethoxy)benzaldehyde and ethyl chloroformate in the presence of sodium chloride and hydrochloric acid. It is then converted into 5-ethoxy-2-mercaptobenzimidazole with sodium hydroxide.</p>Formula:C9H10N2OSPurity:Min. 95%Color and Shape:PowderMolecular weight:194.25 g/mol





