151642-11-4 Usage
Description
1-(2-benzylaminoethyl)-1H-imidazole is a chemical compound with the molecular formula C12H15N3, belonging to the imidazole family and featuring a benzylaminoethyl group. It is widely utilized in research and pharmaceutical applications, serving as a fundamental building block in the synthesis of various pharmaceuticals and bioactive compounds. Its unique structural features and pharmacological properties make it a promising candidate for drug discovery and development. Furthermore, 1-(2-benzylaminoethyl)-1H-imidazole may exhibit biological activities, garnering attention in medicinal chemistry and pharmacology.
Uses
Used in Pharmaceutical Applications:
1-(2-benzylaminoethyl)-1H-imidazole is used as a building block for the synthesis of pharmaceuticals and bioactive compounds, due to its unique structural features and potential pharmacological properties.
Used in Research and Development:
In the field of drug discovery and development, 1-(2-benzylaminoethyl)-1H-imidazole is used as a key component in the creation of novel compounds with potential therapeutic applications.
Used in Medicinal Chemistry:
1-(2-benzylaminoethyl)-1H-imidazole is utilized as a subject of interest for its potential biological activities, contributing to the advancement of medicinal chemistry.
Used in Pharmacology:
1-(2-benzylaminoethyl)-1H-imidazole is also used in pharmacology to study its interactions with biological systems and its potential effects on various physiological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 151642-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,6,4 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 151642-11:
(8*1)+(7*5)+(6*1)+(5*6)+(4*4)+(3*2)+(2*1)+(1*1)=104
104 % 10 = 4
So 151642-11-4 is a valid CAS Registry Number.
151642-11-4Relevant articles and documents
Method for catalyzing aldol self-condensation reaction of low-carbon aldehyde by acid alkali double-function ionic liquid
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, (2018/03/01)
The invention relates to a method for catalyzing aldol self-condensation reaction of low-carbon aldehyde by acid alkali double-function ionic liquid. The method comprises the following steps: adding low-carbon aldehyde and an acid alkali double-function ionic liquid catalyst into a high-pressure kettle, reacting at 60 to 150 DEG C for 1 to 12 hours, and performing hydroxyaldehyde self-condensationreaction on the low-carbon aldehyde to obtain long-chain unsaturated aldehyde, wherein the acid alkali double-function ionic liquid is the acid alkali double-function ionic liquid with cation and anion containing acid and alkali groups correspondingly, or the novel acid alkali double-function ionic liquid with cation containing acid and alkali groups. The method is applied to aldol self-condensation reaction of n-butanal and n-pentanal and is mild in reaction condition, high in catalytic activity and high in selectivity; and the acid alkali double-function ionic liquid catalyst can be reused.
