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5-methyl-1-tosyl-1H-benzo[d]imidazol-2(3H)-one is a complex organic chemical compound with the molecular formula C15H14N2O3S. It is a derivative of benzo[d]imidazol-2(3H)-one, featuring a methyl group at the 5-position and a tosyl (tosylate) group at the 1-position. 5-methyl-1-tosyl-1H-benzo[d]imidazol-2(3H)-one is characterized by its unique structure, which includes a benzene ring fused to an imidazole ring, with the tosyl group providing an additional functional group. It is often used in chemical research and synthesis due to its reactivity and potential applications in the development of pharmaceuticals and other specialty chemicals. The compound's properties, such as solubility and stability, can be influenced by the presence of the tosyl group, making it a valuable intermediate in organic synthesis.

3968-05-6

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3968-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3968-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,6 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3968-05:
(6*3)+(5*9)+(4*6)+(3*8)+(2*0)+(1*5)=116
116 % 10 = 6
So 3968-05-6 is a valid CAS Registry Number.

3968-05-6Upstream product

3968-05-6Downstream Products

3968-05-6Relevant academic research and scientific papers

Electrochemical access to benzimidazolone and quinazolinone derivatives: Via in situ generation of isocyanates

Saha, Debarshi,Taily, Irshad Maajid,Naik, Sumitra,Banerjee, Prabal

, p. 631 - 634 (2021)

Isocyanates are the key intermediates for several organic transformations towards the synthesis of diverse pharmaceutical targets. Herein, we report the development of an oxidant-free protocol for electrochemical in situ generation of isocyanates. This strategy highlights expedient access to benzimidazolones and quinazolinones and eliminates the need for exogenous oxidants. Furthermore, detailed mechanistic studies provide strong support towards our hypothesis of in situ isocyanate generation. This journal is

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