46055-62-3 Usage
Chemical Class
Benzimidazoles
Explanation
1H-Benzimidazol-5-amine,2-ethyl-(9CI) belongs to the class of benzimidazoles, which are heterocyclic compounds containing a benzene ring fused to an imidazole ring.
Explanation
This specific compound is characterized by the presence of an ethyl group attached to the second position of the benzimidazole ring.
Explanation
It is used in various industrial and scientific applications, including as a building block in the synthesis of pharmaceuticals and agrochemicals.
Explanation
Its molecular structure and properties make it suitable for use in organic synthesis and as a starting material for the preparation of diverse chemical derivatives.
Explanation
1H-Benzimidazol-5-amine,2-ethyl-(9CI) is used as a starting material for the preparation of diverse chemical derivatives with potential biological activities.
Explanation
The molecular formula of 1H-Benzimidazol-5-amine,2-ethyl-(9CI) is C9H11N3, indicating the presence of 9 carbon atoms, 11 hydrogen atoms, and 3 nitrogen atoms.
Explanation
The compound is identified by the CAS Registry Number 9CI, which is a unique identifier assigned to chemical compounds.
Explanation
As a heterocyclic compound, 1H-Benzimidazol-5-amine,2-ethyl-(9CI) is generally soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO).
Explanation
The compound is considered stable under normal conditions, such as room temperature and pressure, and in the absence of strong acids, bases, or oxidizing agents.
Explanation
The material provided does not include information about the melting point of 1H-Benzimidazol-5-amine,2-ethyl-(9CI).
Structure
Ethyl group at the second position
Industrial Applications
Building block in synthesis
Molecular Structure
Suitable for organic synthesis
Potential Biological Activities
Preparation of chemical derivatives
CAS Registry Number
9CI
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Melting Point
Not provided
Check Digit Verification of cas no
The CAS Registry Mumber 46055-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,0,5 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 46055-62:
(7*4)+(6*6)+(5*0)+(4*5)+(3*5)+(2*6)+(1*2)=113
113 % 10 = 3
So 46055-62-3 is a valid CAS Registry Number.
46055-62-3Relevant academic research and scientific papers
New antibacterial diazotized derivatives of 5-amino azaheterocycles
Gondal, Humaira Yasmeen,Ali, Muhammad
, p. 1343 - 1348 (2014/01/06)
Six new diazotized derivatives of pharmacologically important azaheterocycles (2a-d, 4a-b) were prepared from their corresponding 5-amino benzimidazoles (1a-d) and benzimidazolones (3a-b). All new compounds have been characterized on the basis of their IR, NMR and Mass spectral data. Antibacterial activity of these compounds is also been reported.
New antibacterial peptide analogs of 5-Aminobenzimidazoles
Gondal, Humaira Y.,Mashooda,Ali, Muhammad
experimental part, p. 650 - 655 (2011/10/08)
Three new peptide analogs 5a-c were obtained through coupling of 5-Amino benzimidazoles 2a-c with L-phenylalanine. For the purpose α-amino group was blocked with phthalic anhydride and activation of α-carboxy group of phenylalanine was carried out by preparing phthaloyl-L-phenylalanyl chloride 4. After developing a successful peptide linkage, the phthaloyl group was removed by treating 5a-c with hydrazine hydrate to get free peptides 6a-c, purified through a column of Amberlite (IR-4B). All of these compounds 2a-c and 5,6a-c have been characterized on the basis of their IR, 1H NMR and EIMS analyses. Antibacterial activity of these compounds is also been reported.
