43215-10-7 Usage
Description
1H-Benzimidazole,1-(methylsulfonyl)-(9CI) is a nitrogen and sulfur-containing heterocyclic compound belonging to the benzimidazole family. It is characterized by its chemical formula C8H9N3O2S and is used as a building block in organic synthesis. The methylsulfonyl group in the compound imparts unique chemical and physical properties, making it useful in various chemical reactions and as a precursor in the synthesis of other compounds. Its potential therapeutic applications, particularly in the field of medicine, are currently being studied, although further research is needed to fully understand its capabilities and properties.
Uses
Used in Organic Synthesis:
1H-Benzimidazole,1-(methylsulfonyl)-(9CI) is used as a building block in organic synthesis for its unique chemical and physical properties. The presence of nitrogen and sulfur atoms in its structure allows it to participate in a variety of chemical reactions, making it a valuable component in the creation of new compounds.
Used in Pharmaceutical Development:
In the field of medicine, 1H-Benzimidazole,1-(methylsulfonyl)-(9CI) is being studied for its potential therapeutic applications. Its unique structure and properties make it a promising candidate for the development of new drugs, although further research is necessary to explore its full potential in this area.
Used in Chemical Reactions:
Due to its nitrogen and sulfur content, 1H-Benzimidazole,1-(methylsulfonyl)-(9CI) is utilized in various chemical reactions. Its ability to participate in different types of reactions makes it a versatile compound in the synthesis of a wide range of products.
Used as a Precursor in Synthesis:
1H-Benzimidazole,1-(methylsulfonyl)-(9CI) serves as a precursor in the synthesis of other compounds, leveraging its unique properties to facilitate the creation of new chemical entities. This role is crucial in advancing the development of novel materials and pharmaceuticals.
Further research is essential to fully understand the potential applications and properties of 1H-Benzimidazole,1-(methylsulfonyl)-(9CI), as its current uses are based on ongoing studies and exploration within the scientific community.
Check Digit Verification of cas no
The CAS Registry Mumber 43215-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,2,1 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 43215-10:
(7*4)+(6*3)+(5*2)+(4*1)+(3*5)+(2*1)+(1*0)=77
77 % 10 = 7
So 43215-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O2S/c1-13(11,12)10-6-9-7-4-2-3-5-8(7)10/h2-6H,1H3
43215-10-7Relevant articles and documents
Synthesis of sulfonamides from azoles and sodium sulfinates at ambient temperature
Fu, Lili,Bao, Xiaodong,Li, Shanshan,Wang, Lingtian,Liu, Zhiguo,Chen, Wanzhi,Xia, Qinqin,Liang, Guang
, p. 2504 - 2511 (2017/04/03)
NBS or NIS mediated direct S[sbnd]N bond formation between azoles and sodium sulfinates is described. The reaction shows good substrate scope and tolerates a wide range of functionalities in both azoles and sodium sulfinate substrates. Pyrazoles are also suitable for this method, various 4-halopyrazoles derivatives were obtained by using N-halosuccinimide (NXS) as the halogen source.
