55000-35-6 Usage
Uses
Used in Organic Synthesis:
[(p-Chlorophenyl)sulfonyl]pyridinioamine anion is used as a reagent in organic synthesis for its ability to act as a nucleophile and react with various electrophiles. This property makes it a valuable component in the creation of complex organic molecules and contributes to its widespread use in the field.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [(p-Chlorophenyl)sulfonyl]pyridinioamine anion is used as a key intermediate in the development of new drugs. Its reactivity and structural features allow for the synthesis of various drug candidates with potential therapeutic applications.
Used in Antimicrobial Applications:
[(p-Chlorophenyl)sulfonyl]pyridinioamine anion has been studied for its potential antimicrobial properties. It is used as an active compound in the development of new antimicrobial agents, aiming to combat drug-resistant bacteria and other pathogens.
Used in Anticancer Applications:
Similarly, [(p-Chlorophenyl)sulfonyl]pyridinioamine anion has been investigated for its potential anticancer properties. It is used as a starting material in the synthesis of novel anticancer drugs, with the goal of developing more effective treatments for various types of cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 55000-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,0 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55000-35:
(7*5)+(6*5)+(5*0)+(4*0)+(3*0)+(2*3)+(1*5)=76
76 % 10 = 6
So 55000-35-6 is a valid CAS Registry Number.
55000-35-6Relevant academic research and scientific papers
Alkene functionalization for the stereospecific synthesis of substituted aziridines by visible-light photoredox catalysis
Yu, Wan-Lei,Chen, Jian-Qiang,Wei, Yun-Long,Wang, Zhu-Yin,Xu, Peng-Fei
supporting information, p. 1948 - 1951 (2018/03/01)
A novel strategy involving visible-light-induced functionalization of alkenes for the synthesis of substituted aziridines was developed. The readily prepared N-protected 1-aminopyridinium salts were used for the generation of N-centered radicals. This approach allowed the synthesis of aziridines bearing various functional groups with excellent diastereoselectivity under mild conditions. Moreover, this protocol was successfully applied to prepare structurally diverse nitrogen-containing frameworks.
Visible-Light-Induced Aza-Pinacol Rearrangement: Ring Expansion of Alkylidenecyclopropanes
Liu, Wen-Deng,Xu, Guo-Qiang,Hu, Xiu-Qin,Xu, Peng-Fei
supporting information, p. 6288 - 6291 (2017/12/08)
A novel visible-light-induced aza-pinacol rearrangement was developed for the first time. In this approach, the addition of the N-centered radical to the C=C bond of alkylidenecyclopropanes delivers a variety of cyclobutanimines and γ-butyrolactones, with
