35342-96-2 Usage
Molecular Structure
A complex organic compound with a benzimidazole ring, a methyl group at position 1, and a substituted phenyl(trimethylsiloxy)methyl group at position 2.
Benzimidazole Ring
A heterocyclic aromatic ring consisting of a 5-membered ring with two nitrogen atoms and a central carbon atom.
Methyl Group (at position 1)
A small alkyl group with one carbon atom and three hydrogen atoms, contributing to the steric and electronic properties of the compound.
Phenyl Ring (part of the substituent)
A 6-membered aromatic ring with alternating single and double carbon-carbon bonds, providing stability and structure to the molecule.
Trimethylsiloxy Group (part of the substituent)
A silicon-based functional group consisting of a silicon atom bonded to three methyl groups and an oxygen atom, contributing to the compound's reactivity and properties.
Substituent
The phenyl(trimethylsiloxy)methyl group attached to the benzimidazole ring, which can influence the compound's chemical properties and reactivity.
Potential Applications
Possible uses in pharmaceuticals, agrochemicals, or materials science due to its unique structure and functional groups.
Further Research
Necessary to fully understand the properties and potential uses of 1-Methyl-2-
benzimidazol, as its complex structure may offer new opportunities in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 35342-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,4 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35342-96:
(7*3)+(6*5)+(5*3)+(4*4)+(3*2)+(2*9)+(1*6)=112
112 % 10 = 2
So 35342-96-2 is a valid CAS Registry Number.
35342-96-2Relevant academic research and scientific papers
Mechanism of Base-Catalyzed Desilylations of Aryl- and Heteroaryltrimethylsilanes
Effenberger, Franz,Spiegler, Wolfgang
, p. 3872 - 3899 (2007/10/02)
The influence of different bases on the cleavage of silicium-carbon bonds in aryl- and heteroaryltrimethylsilanes is investigated in the presence of benzaldehyde as electrophilic scavenger for the aryl and heteroaryl anions formed in this process.A reactivity gradation of the various basic catalysts employed is determined from the reactions with 2-(trimethylsilyl)benzothiazole (1).The increase of catalytic activity of the anions parallels that of their ion potential.Attack of the base at the Si atom is postulated as the first step in this reaction sequence, with subsequent dissociation of the pentacoordinated intermediate in the rate-determining step.The carbanion thus liberated rapidly reacts with benzaldehyde.In the differently substituted aryltrimethylsilanes 13, 13', and 13'' the dependency of aryl anion stability in the base-catalyzed carbodesilylation was investigated.The relative rates of reaction correlate with Hammett's ?-constants rather than with the corresponding aryl anion stabilities.
