92262-91-4 Usage
Uses
Used in Organic Synthesis:
(2-nitronaphtho[2,1-b]furan-7-yl)acetic acid is used as a building block in organic synthesis for its unique structural features, including the presence of a nitro group and a carboxylic acid group. These functional groups can be utilized in various chemical reactions to form a range of complex organic molecules.
Used in Drug Discovery:
In the pharmaceutical industry, (2-nitronaphtho[2,1-b]furan-7-yl)acetic acid is used as a potential lead compound in drug discovery. Its distinct chemical structure may offer novel therapeutic properties, and further research could reveal its potential as a precursor to new medications.
Used in Chemical Research:
(2-nitronaphtho[2,1-b]furan-7-yl)acetic acid serves as a subject of study in chemical research to understand its reactivity, stability, and behavior under different conditions. This knowledge can contribute to the development of safer handling protocols and innovative applications in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 92262-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,6 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92262-91:
(7*9)+(6*2)+(5*2)+(4*6)+(3*2)+(2*9)+(1*1)=134
134 % 10 = 4
So 92262-91-4 is a valid CAS Registry Number.
92262-91-4Relevant academic research and scientific papers
Synthesis of 2-nitronaphtho [2,1-b] furan carboxylic acids derivatives
Einhorn,Lamotte,Buisson,et al.
, p. 143 - 147 (2007/10/02)
2-Nitro naphthofurans carrying a carboxyl group, an acetyl or oxy acetyl chain outer homocycle are obtained - either directly or through their ester - by condensations of bromonitromethane with suitably substituted ortho hydroxy naphthoic aldehydes. 2-Nitro naphthofuran, which bears an acetyl chain on the second carbon of its heterocycle, is formed by direct nitration of the acid or of a (naphtho[2,1-b]-3-furyl)-ecetic ester. These acids and their corresponding esters are nearly always less active against bacteria and protozoa than the reference 2-nitro naphthofurans.
