250651-52-6 Usage
Molecular weight
162.19 g/mol The relative molecular mass of the compound, based on the atomic weights of the constituent elements.
Functional groups
Methanol and methyl group The compound contains a hydroxyl group (-OH) attached to a methanol group (-CH3OH) and a methyl group (-CH3) attached to the alpha carbon of the imidazole ring.
Stereochemistry
2D structure The compound has a two-dimensional structure, with the pyridine and imidazole rings being planar and fused together.
Physical state
Solid The compound is typically found as a solid at room temperature.
Applications
Pharmaceutical industry as a building block for the synthesis of various pharmaceutical drugs and compounds This highlights the compound's primary use in the development of new drugs and therapeutic agents.
Research value
Valuable for medicinal and research purposes, particularly in the development of novel drugs with potential therapeutic applications The unique structure and properties of the compound make it an important tool in the field of medicinal chemistry and drug discovery.
Use as a reagent
Organic synthesis for the preparation of various compounds with diverse functional groups The compound can be used as a reagent in organic synthesis, allowing for the preparation of a wide range of compounds with different functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 250651-52-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,6,5 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 250651-52:
(8*2)+(7*5)+(6*0)+(5*6)+(4*5)+(3*1)+(2*5)+(1*2)=116
116 % 10 = 6
So 250651-52-6 is a valid CAS Registry Number.
250651-52-6Relevant articles and documents
Lithium bromide catalyzed solvent free method for synthesis of 2-substituted benzimidazoles and imidazopyridines
Dekhane, Deepak V.,Pawar, Shivaji S.,Gupta, Sunil V.,Shingare, Murlidhar S.,Thore, Shivaji N.
experimental part, p. 519 - 523 (2011/01/13)
The first successful lithium bromide mediated solvent free condensation of arylenediamine and esters to obtain 2-substituted benzimidazole and imidazopyridine in good to excellent yields is described.
Synthesis and some reactions of 2-acetylimidazo[4,5-b]pyridine. Antituberculotic activity of the obtained compounds
Bukowski,Janowiec,Zwolska-Kwiek,Andrzejczyk
, p. 651 - 654 (2007/10/03)
2-Acetylimidazo[4,5-b]pyridine was prepared and its reactions with some aromatic amines and sulfur (Willgerodt-Kindler reaction), some aromatic aldehydes, some carboxylic acid hydrazides as well as thiourea were investigated. New imidazo[4,5-b]pyridine derivatives with different substituents in 2-position (N-arylthioamides, imines, α β-unsaturated ketones, hydrazido-hydrazones and aminothiazole) were obtained. Most of the synthesized compounds were tested in vitro for their antituberculotic activity.