132430-59-2 Usage
Description
1-benzyl-5-bromo-1H-imidazole is a chemical compound with the molecular formula C10H9BrN2, belonging to the imidazole family. It features a benzyl group and a bromine atom, which contribute to its unique chemical properties and potential applications. 1-benzyl-5-bromo-1H-imidazole is known for its potential biological activity and has been the subject of research in various fields, including organic synthesis, pharmaceuticals, antimicrobial and antifungal properties, and material science.
Uses
Used in Organic Synthesis:
1-benzyl-5-bromo-1H-imidazole is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure allows for versatile reactions and the formation of new molecules with potential applications in different industries.
Used in Pharmaceutical Research:
1-benzyl-5-bromo-1H-imidazole is used as a research compound in pharmaceuticals due to its potential biological activity. It has been studied for its antimicrobial and antifungal properties, making it a promising candidate for the development of new drugs to combat infections.
Used in Antimicrobial Applications:
1-benzyl-5-bromo-1H-imidazole is used as an antimicrobial agent for its ability to inhibit the growth of bacteria and other microorganisms. Its unique chemical structure allows it to target specific cellular processes, making it a valuable tool in the fight against antibiotic-resistant strains.
Used in Antifungal Applications:
1-benzyl-5-bromo-1H-imidazole is used as an antifungal agent to combat fungal infections. Its potential to disrupt fungal cell growth and reproduction makes it a promising candidate for the development of new antifungal drugs.
Used in Material Science:
1-benzyl-5-bromo-1H-imidazole is used in material science for its ability to form metal complexes and coordination polymers. These properties make it a valuable component in the development of new materials with unique properties and potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 132430-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,3 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132430-59:
(8*1)+(7*3)+(6*2)+(5*4)+(4*3)+(3*0)+(2*5)+(1*9)=92
92 % 10 = 2
So 132430-59-2 is a valid CAS Registry Number.
132430-59-2Relevant articles and documents
A general, practical palladium-catalyzed cyanation of (hetero)aryl chlorides and bromides
Senecal, Todd D.,Shu, Wei,Buchwald, Stephen L.
supporting information, p. 10035 - 10039 (2013/10/01)
Playing it safe: The nontoxic cyanide source K4[Fe(CN) 6]×3 H2O can be used for the cyanation of (hetero)aryl halides. The application of palladacycle catalysts prevents poisoning during catalyst formation, thereby allowing for low catalyst loadings, fast reaction times, and wide heterocyclic substrate scope.
Alkylation, Acylation and Silylation of Azoles
Begtrup, Mikael,Larsen, Peter
, p. 1050 - 1057 (2007/10/02)
Performing alkylation, acylation and silylation reactions in separate deprotonation and nucleophilic displacement steps allows for better control of reaction conditions and facilitates problem handling in these processes.In the alkylation of azoles the alkylating agents and solvents possess individual reaction capabilities which seem to be approximately additive.Monoalkylation occurs if the sum of the normalized reaction potentials is equal or larger than the pKa value of the azole.Dialkylation is avoided by keeping the sum of the normalized reaction potentials below the pKa value of the alkylazole.The applicability of these principles is demonstrated by the development of effective procedures for the methylation, benzylation, acetylation, methoxycarbonylation and trimethylsilylation of azoles.
