5714-17-0 Usage
Description
5-Chloro-4-nitrobenzofurazane, also known as 5-Chloro-4-nitro-2,1,3-benzoxadiazole, is a nitrofurazane derivative with a chemical structure that features a benzene ring fused with a furan and a benzene ring, along with a chlorine atom and a nitro group. It is known for its potential antibacterial, antimycotic, and anti-inflammatory properties, making it a compound of interest in various applications.
Uses
Used in Pharmaceutical Industry:
5-Chloro-4-nitrobenzofurazane is used as a pharmaceutical compound for its potential antibacterial properties, which can be utilized in the development of new antibiotics to combat bacterial infections. Its antimycotic properties also make it a candidate for treating fungal infections.
Used in Anti-Inflammatory Applications:
Due to its anti-inflammatory properties, 5-Chloro-4-nitrobenzofurazane can be used as an active ingredient in the development of anti-inflammatory drugs, which can be beneficial in managing conditions such as arthritis, tendinitis, and other inflammatory disorders.
Used in Cosmetics Industry:
In the cosmetics industry, 5-Chloro-4-nitrobenzofurazane may be used as an ingredient in anti-inflammatory and antimicrobial products, such as creams, lotions, and ointments, to help soothe and protect the skin from infections and inflammation.
Used in Agricultural Industry:
The antibacterial and antimycotic properties of 5-Chloro-4-nitrobenzofurazane can also be applied in the agricultural industry for the development of pesticides and fungicides to protect crops from diseases and pests, thereby increasing crop yield and quality.
Check Digit Verification of cas no
The CAS Registry Mumber 5714-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5714-17:
(6*5)+(5*7)+(4*1)+(3*4)+(2*1)+(1*7)=90
90 % 10 = 0
So 5714-17-0 is a valid CAS Registry Number.
5714-17-0Relevant articles and documents
σ-Adduct formation and oxidative substitution in the reactions of 4-nitrobenzofurazan and some derivatives with hydroxide ions in water
Crampton, Michael R.,Lunn, Rachel E.A.,Lucas, David
, p. 3438 - 3443 (2007/10/03)
The reactions of hydroxide ions with 4-nitrobenzofurazan, 1a, 4-nitrobenzofuroxan, 1b, and with three 4-nitro-7-substituted benzofurazans have been examined using 1H NMR and UV-visible spectroscopies. In each case initial reaction is at the 5-position to give an anionic σ-adduct. Kinetic and equilibrium results are reported. NMR spectra show that in the case of la oxidation of the anionic adduct yields 4-nitro-5-hydroxybenzofurazan. In the case of 1b rearrangement of the 5-hydroxy adduct to the thermodynamically more stable 7-hydroxy adduct, possibly by a Boulton-Katritzky mechanism, precedes oxidation. When the 7-substituent in the 4-nitrobenzofurazan is Cl, OMe or OPh the eventual product is 7-hydroxy-4-nitrobenzofurazan produced by nucleophilic displacement of the substituent.
