Related Products of 4857-06-1In 2019 ,《High yielding protocol for direct conversion of thiols to sulfonyl chlorides and sulfonamides》 was published in Journal of Sulfur Chemistry. The article was written by Sohrabnezhad, Samira; Bahrami, Kiumars; Hakimpoor, Farahman. The article contains the following contents:
A new method for oxidative chlorination of thiols RSH [R = CH3(CH2)7, 2-naphthyl, cyclohexyl, ClSO2(CH2)3, etc.] to sulfonyl chlorides RSO2Cl and sulfonamides RSO2N(R1)R2 [R1 = H, C6H5, CH3CH2; R2 = cyclohexyl, 1-naphthyl, CH3CH2, etc.; R1R2 = -CH2(CH2)3CH2-] using H2O2 in the presence of TMSCl is reported. The excellent yields, short reaction times, excellent efficiencies, low costs, and easy separation of products are the most important advantages of this method. In addition to this study using 2-Chloro-1H-benzo[d]imidazole, there are many other studies that have used 2-Chloro-1H-benzo[d]imidazole(cas: 4857-06-1Related Products of 4857-06-1) was used in this study.
2-Chloro-1H-benzo[d]imidazole(cas: 4857-06-1) is an analog of benzimidazole that has been synthesized by Langmuir adsorption isotherm. It is a white crystalline solid that can be dissolved in water and hydrochloric acid. 2-Chloro-1H-benzo[d]imidazole inhibits the growth of herpes simplex virus by acting as a competitive inhibitor for the viral enzyme thymidine kinase, which catalyzes the conversion of thymine to thymidine.Related Products of 4857-06-1
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem