329082-06-6 Usage
Chemical compound
2-(4,5-dimethoxy-2-nitrophenyl)-1H-benzo[d]imidazole This compound 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 articles and documents
Hypervalent iodine promoted: Ortho diversification: 2-aryl benzimidazole, quinazoline and imidazopyridine as directing templates
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