103747-88-2 Usage
Description
1-(2,3-DIMETHYL-3H-IMIDAZOL-4-YL)-ETHANONE is a chemical compound with the molecular formula C7H10N2O. It is a ketone derivative and belongs to the imidazole class of compounds. 1-(2,3-DIMETHYL-3H-IMIDAZOL-4-YL)-ETHANONE is characterized by its unique structure, which includes a 3H-imidazol-4-yl moiety, a common pharmacophore found in many medicinal compounds. Its diverse reactivity and potential biological activities make it a compound of interest in various research fields, particularly in organic synthesis and pharmaceutical research.
Uses
Used in Organic Synthesis:
1-(2,3-DIMETHYL-3H-IMIDAZOL-4-YL)-ETHANONE is used as a building block in organic synthesis for the creation of various biologically active compounds. Its unique structure and reactivity make it a valuable component in the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2,3-DIMETHYL-3H-IMIDAZOL-4-YL)-ETHANONE is used as a key component in the synthesis of medicinal compounds. Its presence in the structure of many biologically active molecules suggests that it may have potential pharmaceutical properties, making it a valuable asset in drug discovery and development.
Used in Drug Discovery:
Due to its potential biological activities and pharmaceutical properties, 1-(2,3-DIMETHYL-3H-IMIDAZOL-4-YL)-ETHANONE is used in drug discovery as a starting point for the development of new drugs. Its unique structure and diverse reactivity allow researchers to explore various avenues in the search for novel therapeutic agents.
Used in Research Fields:
1-(2,3-DIMETHYL-3H-IMIDAZOL-4-YL)-ETHANONE is also used in various research fields beyond organic synthesis and pharmaceutical research. Its potential applications in drug discovery and development, as well as its unique structure, make it a compound of interest for further exploration and study.
Check Digit Verification of cas no
The CAS Registry Mumber 103747-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,4 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103747-88:
(8*1)+(7*0)+(6*3)+(5*7)+(4*4)+(3*7)+(2*8)+(1*8)=122
122 % 10 = 2
So 103747-88-2 is a valid CAS Registry Number.
103747-88-2Relevant articles and documents
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.
