5338-40-9 Usage
Benzimidazole class
1-C-1H-benzimidazol-2-ylpentitol belongs to the benzimidazole class of organic compounds, which are known for their diverse biological activities.
Benzimidazole core structure
The compound features a benzimidazole core, which is formed by the fusion of a benzene ring and an imidazole ring.
Pentitol side chain
1-C-1H-benzimidazol-2-ylpentitol has a pentitol side chain attached to the benzimidazole core, which may influence its biological activity and interactions.
Biological processes
Benzimidazole compounds, including this specific compound, have been implicated in various biological processes such as cell growth, apoptosis, and DNA binding.
Potential applications
Although the specific properties and applications of 1-C-1H-benzimidazol-2-ylpentitol have not been fully explored, it may hold promise as a potential pharmaceutical or biochemical reagent due to its unique structure and biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 5338-40-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5338-40:
(6*5)+(5*3)+(4*3)+(3*8)+(2*4)+(1*0)=89
89 % 10 = 9
So 5338-40-9 is a valid CAS Registry Number.
5338-40-9Relevant articles and documents
Using molecular iodine in direct oxidative condensation of aldoses with diamines: An improved synthesis of aldo-benzimidazoles and aldo-naphthimidazoles for carbohydrate analysis
Lin, Chunchi,Lai, Po-Ting,Liao, Sylvain Kuo-Shiang,Hung, Wei-Ting,Yang, Wen-Bin,Fang, Jim-Min
, p. 3848 - 3853 (2008/09/21)
(Chemical Equation Presented) A practical method has been developed for conversion of unprotected and unmodified aldoses to aldobenzimidazoles and aldo-naphthimidazoles. Using iodine as an oxidant or promoter in acetic acid solution, a series of mono-, di-, and trialdoses, including those containing carboxyl and acetamido groups, undergo an oxidative condensation reaction with o-phenylenediamine or 2,3-naphthalenediamine at room temperature to give the aldo-benzimidazole and aldo-naphthimidazole products in high yields. No cleavage of the glycosidic bond occurs under such mild reaction conditions. The composition analysis of saccharides is realized by the HPLC analysis of the fluorescent naphthimidazole derivatives.
