78288-57-0 Usage
Aromatic amine category
It is classified as an aromatic amine due to the presence of the benzimidazole ring and the amine functional group (-NH2).
Benzimidazole ring
The core structure of this compound is a benzimidazole ring, which is a heterocyclic aromatic ring system consisting of a 5-membered ring with two nitrogen atoms and one benzene ring fused to it.
Methyl group attachment
Two methyl groups (-CH3) are attached to the 5th and 6th carbon atoms of the benzimidazole ring, which influences the compound's properties and reactivity.
Biological activities
This compound has been found to exhibit various biological activities, such as antiviral and antitumor properties, making it a potential candidate for pharmaceutical applications.
Synthesis of other organic compounds
1H-Benzimidazol-1-amine, 5,6-dimethyl-(9CI) can be used as a starting material or building block in the synthesis of other organic compounds, contributing to the development of new molecules with potential applications.
Drug discovery and development
Due to its versatile chemical properties and potential therapeutic applications, this compound is utilized in drug discovery and development processes to create new and effective pharmaceuticals.
Research applications
The compound is commonly used in research settings to study its properties, reactivity, and potential applications in various fields, including medicinal chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 78288-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,2,8 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78288-57:
(7*7)+(6*8)+(5*2)+(4*8)+(3*8)+(2*5)+(1*7)=180
180 % 10 = 0
So 78288-57-0 is a valid CAS Registry Number.
78288-57-0Relevant articles and documents
Amination of heterocyclic compounds with O-benzoylhydroxylamine derivatives
Parlanti, Luca,Discordia, Robert P.,Hynes Jr., John,Miller, Michael M.,O'Grady, Harold R.,Shi, Zhongping
, p. 3821 - 3824 (2008/02/12)
The N-amination of heterocyclic compounds 1a - k with O- benzoylhydroxylamine derivatives 5 was developed and demonstrated to be a superior alternative to existing N-amination methods. A structure - reactivity relationship study was performed on variously
