59938-40-8 Usage
Description
3-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde is a heterocyclic chemical compound with the molecular formula C8H5BrN2O. It features an imidazole ring fused to a pyridine ring, with a bromine atom attached to the imidazole and an aldehyde group on the pyridine. 3-bromoimidazo[1,2-a]pyridine-2-carbaldehyde is recognized for its role in organic synthesis and its potential biological activities, such as antimicrobial and antitumor properties, making it a significant intermediate in the development of pharmaceutical compounds and complex organic molecules.
Uses
Used in Organic Synthesis:
3-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde is utilized as a building block in organic synthesis for the preparation of complex molecules and pharmaceutical compounds. Its unique structure allows for the creation of a variety of derivatives with diverse applications in chemical research and development.
Used in Pharmaceutical Compounds:
In the pharmaceutical industry, 3-bromoimidazo[1,2-a]pyridine-2-carbaldehyde is used as a key intermediate in the synthesis of drugs. Its presence in the molecular structure can contribute to the compound's therapeutic properties, such as enhancing the effectiveness of medications or improving their pharmacokinetic profiles.
Used in Drug Discovery:
3-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde is employed in drug discovery processes for its potential biological activities. Its antimicrobial and antitumor properties are of particular interest, as they can lead to the development of new treatments for various diseases and conditions.
Used in Antimicrobial Agents:
3-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde is used as an antimicrobial agent for its ability to combat microbial infections. Its chemical structure allows it to interact with microbial cells, inhibiting their growth and contributing to the development of new antimicrobial therapies.
Used in Antitumor Research:
In the field of antitumor research, 3-bromoimidazo[1,2-a]pyridine-2-carbaldehyde is used to explore its potential as an antitumor agent. Its capacity to affect tumor cells and potentially inhibit cancer growth makes it a valuable compound in the search for novel cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 59938-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,3 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59938-40:
(7*5)+(6*9)+(5*9)+(4*3)+(3*8)+(2*4)+(1*0)=178
178 % 10 = 8
So 59938-40-8 is a valid CAS Registry Number.
59938-40-8Relevant articles and documents
Synthesis of new substituted imidazo[1,2-a]pyridinylpropenenitriles through sequential one-pot Suzuki–Miyaura/Knoevenagel reactions in aqueous medium
Bakhta, Saléha,Kabri, Youssef,Crozet, Maxime D.,Nedjar-Kolli, Bellara,Vanelle, Patrice
, p. 2561 - 2571 (2019)
A series of imidazo[1,2-a]pyridinylpropenenitriles were synthesized via consecutive one-pot Suzuki–Miyaura and Knoevenagel reactions in water/ethanol mixture between imidazo[1,2-a]pyridine-2-carbaldehydes, arylboronic acids and malononitrile, methyl cyanoacetate or ethyl cyanoacetate. This environmental friendly procedure tolerates a wide range of boronic acids and affords a new substituted imidazo[1,2-a]pyridinyl propenenitriles in good yields under microwave irradiation.
Pyrrolization processes of vinyl substituted imidazo[1,2-a]pyridine, pyrimidine and 1,8-naphthyridine
Chavignon,Teulade,Madesclaire,Gueiffier,Blache,Viols,Chapat,Dauphin
, p. 691 - 697 (2007/10/02)
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