329082-06-6 Usage
Chemical compound
2-(4,5-dimethoxy-2-nitrophenyl)-1H-benzo[d]imidazole 2-(4,5-dimethoxy-2-nitrophenyl)-1H-benzo[d]imidazole is a derivative of 1H-benzo[d]imidazole with specific substituents attached to its structure.
Derivative of 1H-benzo[d]imidazole
2-(4,5-dimethoxy-2-nitrophenyl)-1H-benzo[d]imidazole It is derived from the base structure of 1H-benzo[d]imidazole, a five-membered aromatic ring system.
Substituents
Two methoxy groups and a nitro group These functional groups are attached to the phenyl ring of the 1H-benzo[d]imidazole core structure.
Potential pharmacological activities
2-(4,5-dimethoxy-2-nitrophenyl)-1H-benzo[d]imidazole The compound has been studied for its possible applications in medicine due to its potential pharmacological properties.
Precursor for synthesis
Nitro group The presence of the nitro group in the compound makes it a potential precursor for the synthesis of other organic compounds.
Complex structure
2-(4,5-dimethoxy-2-nitrophenyl)-1H-benzo[d]imidazole The compound has a complex structure that requires expertise in organic synthesis to handle and manipulate.
Potential reactivity
2-(4,5-dimethoxy-2-nitrophenyl)-1H-benzo[d]imidazole Due to its complex structure and functional groups, the compound may exhibit potential reactivity, necessitating careful consideration in its usage and handling.
Check Digit Verification of cas no
The CAS Registry Mumber 329082-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,0,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 329082-06:
(8*3)+(7*2)+(6*9)+(5*0)+(4*8)+(3*2)+(2*0)+(1*6)=136
136 % 10 = 6
So 329082-06-6 is a valid CAS Registry Number.
329082-06-6Relevant academic research and scientific papers
Saha, Moumita,Das, Asish R.
, p. 941 - 955 (2020)
The mild and efficient palladium-catalyzed ortho C(sp2)-H diversification of (NH)-free 2-substituted benzimidazole, quinazoline, and imidazopyridine is reported using hypervalent iodine as the key reagent. Acetoxy, aryl, iodide and nitro functi
Efficient method for the synthesis of benzimidazoquinazoline derivatives with three-point diversity
Saha, Biswajit,Sharma, Sunil,Kundu, Bijoy
, p. 3455 - 3470 (2008/02/13)
An efficient strategy for the preparation of a novel heterocyclic ring system of benzimidazoquinazolines with three-point diversity has been described. The compounds were obtained by treating o-phenylene diamines with o-nitrobenzaldehyde to give benzimidazoles, followed by reduction of the nitro group to give an amine. Derivatization of the resulting amine with isothiocyanates followed by in situ cyclodesulfurization at rt furnished the title compounds in high yields and purities. Copyright Taylor & Francis Group, LLC.
