63875-31-0Relevant academic research and scientific papers
Synthesis of some new nucleosides derived from 2-mercapto benzimidazole with expected biological activity
Amer, Hamada H.,Ali, Omar M.,El-Kafaween, Ibrahim Kh.
, p. 2303 - 2310 (2017)
2-mercaptobenzimidazole derivatives and their acyclic nucleosides were synthesized. The synthesized compounds were tested for their antibacterial activity against Escherichia coli, Staphylococcus aureus and S. epidermidis. Most of tested compounds showed
Synthesis of 2-mercaptobenzimidazole derivatives as potential anti-microbial and cytotoxic agents
Hosamani, Kallappa M.,Shingalapur, Ramya V.
experimental part, p. 311 - 319 (2011/11/05)
A series of novel 2-(1H-benzimidazol-2-ylsulfanyl)-N-(4-oxo-2-phenyl- thiazolidin-3yl)-acetamide 5a-j have been synthesized from various aldehydes and 2-(5-phenyl-[1,3,4]-oxadiazol-2-ylmethylsulfanyl)-1H-benzimidazole 6a-j from various benzoic acids. Thes
Synthesis and characterization of lanthanide(III) nitrate complexes with Terdentate ONO donor hydrazone derived from 2-benzimidazolyl mercaptoaceto hydrazide and o-hydroxy aromatic aldehyde
Naik, Vinayak M.,Mallur, Nirmalkumar B.
experimental part, p. 1900 - 1910 (2012/05/31)
A few eight coordinated complexes of lanthanide(III) nitrate with 2-benzimidazolyl mercaptoaceto hydrazone ligand (LH2) with the general formula [Ln(LH)2NO3]H2O (where Ln = La, Pr, Nd, Sm and Gd) have been synth
Derivatives of benzimidazole pharmacophore: Synthesis, anticonvulsant, antidiabetic and DNA cleavage studies
Shingalapur, Ramya V.,Hosamani, Kallappa M.,Keri, Rangappa S.,Hugar, Mallinath H.
experimental part, p. 1753 - 1759 (2010/06/17)
In seeking broad spectrum pharmacological activities of benzimidazole derivatives, a group of 4-thiazolidinones 5(a-j) and 1,3,4-oxadiazoles 6(a-j) containing 2-mercapto benzimidazole moiety were synthesized and screened for in vivo anticonvulsant activit
Synthesis, spectral and thermal studies of tin(IV) complexes using 2-benzimidazolylmercaptoaceto hydrazone type of ligands
Naik,Patil,Tallur,Mallur
experimental part, p. 22 - 25 (2009/04/06)
The metal complexes of SnIV with 2-benzimidazolylmercaptoaceto hydrazones of 1:2 metal to ligand stoichiometry have been synthesized. Molar conductance data reveal their non-electrolytic nature. The spectral studies show that the ligands react
Synthesis, spectroscopic and thermal studies of bivalent transition metal complexes with the hydrazone derived from 2-benzimidazblyl mercaptoaceto hydrazide and o-hydroxy aromatic aldehyde
Naik,Sambrani,Mallur
experimental part, p. 1793 - 1797 (2009/07/25)
Syntheses of complexes of a few first transition series bivalent metal ions like Co(II), Ni(II) and Cu(II) complexes with 2-benzimidazolyl mercaptoaceto hydrazone have been reported. The complexes have been characterized on the basis of analytical, molar
Green route for the heterocyclization of 2-mercaptobenzimidazole into β-lactum segment derivatives containing -CONH- bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms
Desai, Krunal G.,Desai, Kishor R.
, p. 8271 - 8279 (2007/10/03)
The efficient and rapid synthesis of novel azetidin-2-ones 4a-j has been established. Thus, both microwave and conventional condensation 2-{(1H-benzimidazol)-ylthio}-N′-2-(substituted phenyl) hydrazide with chloroacetylchloride were carried out in DMF-ben
Synthesis and characterization of niobium(V) complexes with terdentate ONO donor hydrazones
Naik,Mallur
, p. 780 - 784 (2007/10/03)
The metal complexes of niobium(V) with 2-benzimidazolyl mercaptoaceto hydrazones have been synthesized in dry alcohol under nitrogen atmosphere and characterized by elemental analyses, molar conductance measurements, infrared, electronic and 1H
Synthesis of 3-(thiadiazol-2-ylthio-, pyridin-2-ylthio- and benzimidazol-2-ylthio)-2H-1-benzopyran-2-ones
Ahluwalia, V K,Tyagi, Renu,Khurana, Anju
, p. 1097 - 1100 (2007/10/02)
The title compounds have been prepared by the reaction of thiadiazol-2-ylthio-, pyridin-2-ylthio- and benzimidazol-2-ylthioacetic acid hydrazides with o-hydroxybenzaldehydes followed by cyclization of the resultant acetylhydrazones in the presence of PPA.
