6098-47-1 Usage
Uses
Used in Pharmaceutical Industry:
N-[3-(methylsulfanyl)-9H-fluoren-2-yl]acetamide is used as a potential pharmaceutical agent due to its unique chemical structure. The presence of the fluorene backbone, thiomethyl group, and acetamide functional group may contribute to its interaction with biological targets, making it a candidate for drug development.
Used in Materials Science:
In the field of materials science, N-[3-(methylsulfanyl)-9H-fluoren-2-yl]acetamide is used for its potential applications in organic electronics. The fluorene backbone, a key component of the compound, is known for its electronic properties, which could be harnessed in the development of advanced materials for electronic devices and components.
Further research is essential to explore the specific applications and optimize the use of N-[3-(methylsulfanyl)-9H-fluoren-2-yl]acetamide in these industries, as well as to discover additional potential uses based on its chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6098-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,9 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6098-47:
(6*6)+(5*0)+(4*9)+(3*8)+(2*4)+(1*7)=111
111 % 10 = 1
So 6098-47-1 is a valid CAS Registry Number.
6098-47-1Relevant academic research and scientific papers
Substituent effects on the bioactivation of 2-(N-hydroxyacetamido)fluorenes by N-arylhydroxamic acid N,O-cyltransferase
Elfarra,Hanna
, p. 1453 - 1460 (2007/10/02)
A series of 7-substituted analogues of 2-(N-hydroxyacetamido)fluorene (1) was subjected to bioactivation by a partially purified preparation of hamster hepatic AHAT, and the rates of methylthio adduct formation resulting from the reaction of the activated intermediates with N-acetylmethionine were determined. Electronegative substituents enhanced the amount of adduct formed; this finding contrasted with the results of a previous study in which it was found that electron-donating substituents facilitated the mechanism-based inactivation of AHAT by analogues of 1. The structures of the adducts formed from reaction of the activated forms of several of the 7-substituted compounds with N-acetylmethionine and with 2'-deoxyguanosine were determined; the types of adducts formed were similar to those formed with electrophiles generated by the AHAT-catalyzed activation of 1. Electronegative substituents enhanced the amount of adducts formed in the reaction with 2'-deoxyguanosine as well as with N-acetylmethionine.
