93111-58-1 Usage
Heterocyclic compound
A compound with a five-membered ring containing both carbon and nitrogen atoms 1H-Imidazole, 1-butyl-2-ethyl-4,5-dihydrofeatures a five-membered ring with three carbon atoms, one nitrogen atom, and one double bond.
Five-membered ring
A ring structure with five atoms The compound has a five-membered ring in its structure, which is characteristic of imidazole derivatives.
One double bond
The presence of a carbon-carbon double bond in the five-membered ring The imidazole ring in 1H-Imidazole, 1-butyl-2-ethyl-4,5-dihydro- contains a double bond, which influences its chemical properties and reactivity.
Organic synthesis
Utilized as a building block for creating more complex organic molecules 1H-Imidazole, 1-butyl-2-ethyl-4,5-dihydrois valuable in organic synthesis due to its ability to form more complex molecules.
Pharmaceutical research
Potential applications in the development of new drugs or materials 1H-Imidazole, 1-butyl-2-ethyl-4,5-dihydro- may have applications in pharmaceuticals due to its unique structure and properties.
Biological activity
Possesses potential biological activity Due to its biological activity, 1H-Imidazole, 1-butyl-2-ethyl-4,5-dihydromay have therapeutic or toxic effects and should be handled with care.
Safety precautions
Proper safety measures should be taken when working with 1H-Imidazole, 1-butyl-2-ethyl-4,5-dihydro- Researchers and handlers should exercise caution and follow safety protocols to minimize risks associated with the compound's potential biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 93111-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,1 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93111-58:
(7*9)+(6*3)+(5*1)+(4*1)+(3*1)+(2*5)+(1*8)=111
111 % 10 = 1
So 93111-58-1 is a valid CAS Registry Number.
93111-58-1Relevant academic research and scientific papers
Nucleophilic Ring Opening of 2-Oxazolines with Amines: A Convenient Synthesis for Unsymmetrically Substituted Ethylenediamines
Fazio, Michael J.
, p. 4889 - 4893 (2007/10/02)
The reaction of 2-alkyl-2-oxazolines with alkyl- and arylamines was investigated.The acid-catalyzed nucleophilic ring opening of the 2-oxazolines yields N-(2-aminoethyl)carboxamides in good to excellent yields with secondary amines and hindered primary amines.The N-(2-aminoethyl)carboxamides were hydrolyzed under acidic or basic conditions to selectively yield unsymmetrically substituted ethylenediamines.
