154112-95-5 Usage
Molecular Structure
The compound consists of a benzimidazole ring and a benzylacetamide group.
Classification
It belongs to the class of organic compounds known as benzimidazoles, which are aromatic compounds containing a benzene ring fused to an imidazole ring.
Usage in Medicinal Chemistry
2-(1H-benzo[d]imidazol-2-yl)-N-benzylacetamide is commonly used in medicinal chemistry, particularly in the development of pharmaceuticals and drugs.
Biological Activities and Therapeutic Properties
The compound has potential biological activities and therapeutic properties, making it a valuable compound in the development of drugs.
Utilization in Chemical Research
The compound is also utilized in chemical research as a building block for the synthesis of various bioactive molecules.
Unique Structure and Functional Groups
The unique structure and functional groups of 2-(1H-benzo[d]imidazol-2-yl)-N-benzylacetamide make it a valuable and versatile compound in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 154112-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,1,1 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154112-95:
(8*1)+(7*5)+(6*4)+(5*1)+(4*1)+(3*2)+(2*9)+(1*5)=105
105 % 10 = 5
So 154112-95-5 is a valid CAS Registry Number.
154112-95-5Relevant academic research and scientific papers
Ukrainets, I. V.,Taran, S. G.,Turov, A. V.
, p. 941 - 944 (1993)
The reaction of N-R-substituted amides of 2-carboxymalonanilic acid with the equimolar amount of o-phenylenediamine was studied under conditions of thermolysis. It was established that the main products of this reaction are the corresponding amides of ben
Elemental Sulfur/DMSO-Promoted Multicomponent One-pot Synthesis of Malonic Acid Derivatives from Maleic Anhydride and Amines
Nguyen, Le Anh,Retailleau, Pascal,Nguyen, Thanh Binh
, p. 2864 - 2869 (2019/05/01)
Malonic acid derivatives could be conveniently prepared with high degree of functional flexibility via redox condensation reactions between anhydride maleic, amines, elemental sulfur and DMSO as oxidant. This multicomponent decarboxylative transformation consists in a cascade of ring opening, decarboxylative oxidative thioamidation at temperature as low as 50 °C. (Figure presented.).
