75815-57-5 Usage
Molecular Structure
1H-Imidazole-4-carboxaldehyde, 5-methyl-1-(phenylmethyl)is composed of an imidazole ring with a carboxaldehyde group at the 4th position, a methyl group at the 5th position, and a phenylmethyl group at the 1st position.
Functional Groups
The compound contains a carboxaldehyde group (-CHO), a methyl group (-CH3), an imidazole ring, and a phenylmethyl group (-CH2-C6H5).
Usage
The chemical is commonly used in organic synthesis and pharmaceutical research as a building block for various compounds and drugs due to its unique and versatile structure.
Chelating Agent
The compound has potential as a chelating agent, which can bind to metal ions and form complexes.
Antimicrobial Properties
The compound has antimicrobial properties, which can be effective against bacteria and other microorganisms.
Antifungal Properties
The compound also has antifungal properties, which can be effective against fungi and other yeasts.
Applications
Due to its unique structure and versatile properties, the compound is a valuable compound for a range of applications in the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 75815-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,1 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75815-57:
(7*7)+(6*5)+(5*8)+(4*1)+(3*5)+(2*5)+(1*7)=155
155 % 10 = 5
So 75815-57-5 is a valid CAS Registry Number.
75815-57-5Relevant academic research and scientific papers
Synthesis of 4(5)-Acyl-, 1-Substituted 5-Acyl, and 1-Substituted 4-Acyl-1H-imidazoles from 4-Aminoisoxazoles
Reiter, Lawrence A.
, p. 2714 - 2726 (2007/10/02)
4-Aminoisoxazoles can be acylated with a wide variety of activated carboxylic acids.Hydrogenation of the resulting amides gives α-(acylamino)enaminones, which cyclize to 4(5)-acylimidazoles upon treatment with base.This method allows for the synthesis of acylimidazoles with a wide range of substituents at C-2.Utilization of N-substituted 4-aminoisoxazoles in the same sequence of reactions yields 1-substituted 5-acylimidazoles, a substitution pattern not otherwise easily prepared.Treatment of α-(acylamino)enaminones, derived from N-unsubstituted isoxazoles, with primary amines leads to incorporation of the amine at the β-position with concomitant expulsion of ammonia.This sequence efficiently yields 1-substituted and 1,2-disubstituted 4-acylimidazoles but does not give satisfactory yields of 5-substituted 4-acylimidazoles due to steric inhibition of the amine exchange.
Cyclic imidazole cyanoguanidines
-
, (2008/06/13)
There are disclosed novel compounds described as imidazole cyanoguanidines in which the imidazole moiety is connected to the cyanoguanidine moiety through a cyclic group which may optionally contain one or two alkylene linkages. The cyclic groups may be p
