86539-70-0 Usage
Description
1-(1-methyl-5-nitronaphtho[2,1-b]furan-2-yl)ethanone, also known as MNF, is a chemical compound characterized by its molecular formula C15H11NO3. It is a yellowish solid with potential applications in various fields due to its unique properties.
Uses
Used in Cellular Imaging:
1-(1-methyl-5-nitronaphtho[2,1-b]furan-2-yl)ethanone is used as a fluorescent staining agent for cellular imaging, allowing for the visualization and analysis of cellular structures and functions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(1-methyl-5-nitronaphtho[2,1-b]furan-2-yl)ethanone is used as a compound with potential pharmacological properties. It is being studied for its ability to inhibit the activity of certain enzymes, which could lead to the development of new drugs targeting specific enzyme pathways.
Used in Organic Synthesis:
1-(1-methyl-5-nitronaphtho[2,1-b]furan-2-yl)ethanone is also used as a building block in the synthesis of organic compounds. Its unique structure makes it a valuable component in the creation of new molecules with various applications.
Safety Precautions:
It is important to handle 1-(1-methyl-5-nitronaphtho[2,1-b]furan-2-yl)ethanone with caution, as it may be hazardous if ingested or inhaled and can cause skin and eye irritation. Proper safety measures should be taken when working with this compound to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 86539-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,3 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86539-70:
(7*8)+(6*6)+(5*5)+(4*3)+(3*9)+(2*7)+(1*0)=170
170 % 10 = 0
So 86539-70-0 is a valid CAS Registry Number.
86539-70-0Relevant articles and documents
Research on nitro-derivatives of biological interest. XXX Methylated 2-nitronaphthofuranes, synthesis and activity against microorganisms
Einhorn,Demerseman,Royer,Cavier
, p. 175 - 180 (2007/10/02)
2-Nitrofuran derivatives methylated on their heterocycle must be prepared after various methods, according to cases. 1-Methyl 2-nitro naphtho [2. 1-b]furan is formed - with a yield of about 35% - by displacing the keton group of 2-acetyl of 2-acetyl 1-methyl naphtho [2. 1-b]furan using nitric acid in acetic acid. 7-Methoxy 1-methyl 2-nitro naphtho [2. 1-b]furan is obtained by treating 7-methoxy 1-methyl naphtho [2. 1-b]furan with a limited quantity of nitric acid in methylene chloride. Yield near to 10%. 3-Methyl 2-nitro naphtho [2. 3-b]furan is only accessible by deshydrogenation of 3-methyl 2-nitro 5.6.7.8-tetrahydro naphtho [2. 3-b]furan - which synthesis was previously described. Finally, 3-methyl 2-nitro naphtho [1. 2-b]furan is elaborated by action of nitric acid in methylene choride on 2-acetyl 3-methyl naphtho [1. 2-b]furan. Approximate yield: 25%. The methyl group added to the 2-nitro-naphthofuran heterocycle enhances the antibacterial and protozoocidal activities when one passes from 2-nitro naphtho [2. 1-b]furan to 1-methyl 2-nitro naphtho [2.1-b]furan. Nevertheless, it strongly decreases the antibacterial activity when one passes from 7-methoxy 2-nitro naphtho [2. 1-b]furan to 7-methoxy 1-methyl 2-nitro naphtho [2. 1-b]furan. The modifications in the activities noticed in the other cases are of less importance.
