14700-66-4 Usage
Uses
Used in Pharmaceutical Industry:
N-Benzyl-1H-imidazol-2-amine is used as a key intermediate for the synthesis of drugs with anti-fungal and anti-inflammatory properties. Its benzyl-attached imidazole structure allows for the development of compounds that can effectively target and treat various fungal infections and inflammatory conditions.
Used in Organic Synthesis:
In the field of organic synthesis, N-Benzyl-1H-imidazol-2-amine is utilized as a building block for the creation of a wide range of organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
N-Benzyl-1H-imidazol-2-amine is employed as a versatile component in medicinal chemistry, where it contributes to the design and development of new pharmaceuticals. Its presence in drug discovery processes aids in the creation of novel therapeutic agents with potential applications in various medical fields.
Used in Coordination Chemistry and Metal Complexes:
N-Benzyl-1H-imidazol-2-amine is also used as a potential ligand in coordination chemistry, where it can form metal complexes. This application allows for the exploration of its properties and potential uses in areas such as catalysis and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 14700-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,0 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14700-66:
(7*1)+(6*4)+(5*7)+(4*0)+(3*0)+(2*6)+(1*6)=84
84 % 10 = 4
So 14700-66-4 is a valid CAS Registry Number.
14700-66-4Relevant academic research and scientific papers
Synthesis of 1H-Imidazoimidazole
Compernolle, Frans,Toppet, Suzanne
, p. 541 - 544 (2007/10/02)
The synthesis and structure analysis of the unknown 1H-imidazoimidazole (1) is described.The preparation involves alkylation of 2-aminoimidazole with bromoacetaldehyde diethyl acetal and subsequent hydrolysis and cyclization with hydrochloric acid.The structure was characterized by mass spectrometry and by 1H-, 15N- and 13C-nmr of 1 and by 1H-nmr of its 1-benzyl derivative 8.An independent synthesis of 8 was accomplished via cyclization of 2-(N-dichloroethyl-N-benzyl)aminoimidazole (11).
