250600-43-2 Usage
Imidazole derivative
Heterocyclic compound with an imidazole core
Imidazoles are a class of heterocyclic compounds that contain a five-membered ring with two nitrogen atoms.
4-Bromophenoxyethyl moiety
Attached to the nitrogen atom
This functional group consists of a phenol group with a bromine atom at the para position (4th position) and an ethyl group attached to the oxygen atom.
Biological activities
Antifungal, anti-inflammatory, and anticancer properties
Imidazoles are known for their diverse biological activities, which may include fighting fungal infections, reducing inflammation, and inhibiting cancer cell growth.
Potential applications
Pharmaceuticals and research
Due to its unique structure and potential biological activities, this compound may be useful in the development of new drugs or as a research tool.
Chemical reactivity
Influenced by the imidazole core and bromophenoxy substituent
The presence of the imidazole core and the bromophenoxy group may confer specific reactivity to this compound, making it a candidate for further chemical modifications or reactions.
Further studies needed
To fully elucidate properties and potential uses
More research is required to understand the compound's properties, reactivity, and potential applications in various fields, such as pharmaceuticals or materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 250600-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,6,0 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 250600-43:
(8*2)+(7*5)+(6*0)+(5*6)+(4*0)+(3*0)+(2*4)+(1*3)=92
92 % 10 = 2
So 250600-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrN2O/c12-10-1-3-11(4-2-10)15-8-7-14-6-5-13-9-14/h1-6,9H,7-8H2
250600-43-2Relevant articles and documents
Palladium-mediated 11C-carbonylations using aryl halides and cyanamide
Nordeman,Chow,Odell,Antoni,Odell
, p. 4875 - 4881 (2017/07/10)
A robust and high-yielding radiochemical synthesis of 11C-N-cyanobenzamides using a palladium-mediated aminocarbonylation with 11C-CO, aryl halides and cyanamide is described. The bidentate ligand 1,1′-bis(diphenylphosphino)ferrocene provided 11C-N-cyanobenzamides from aryl-iodides, bromides, triflates and even chlorides in 28-79% radiochemical yield after semi-preparative HPLC. To further highlight the utility of this method, novel 11C-N-cyanobenzamide analogs of flufenamic acid, meflanamic acid, dazoxiben and tamibarotene were synthesized in 34-71% radiochemical yields.
