637-61-6

Usage

Uses

Used in Organic Synthesis:
N-Chloro-p-benzoquinoneimine is utilized as an oxidizing and chlorinating agent in organic synthesis, facilitating various chemical reactions and transformations.
Used in Industrial Applications:
N-CHLORO-P-BENZOQUINONEIMINE is employed in industrial settings for its oxidizing and chlorinating capabilities, contributing to the production process of different products.
Used in Healthcare Settings:
N-Chloro-p-benzoquinoneimine is used as a potent antimicrobial agent in healthcare settings, playing a crucial role in disinfection and sterilization processes to ensure a hygienic environment.
Used in Water Treatment Facilities:
In water treatment, N-CHLORO-P-BENZOQUINONEIMINE is applied for its antimicrobial properties to ensure the safety and cleanliness of water supplies.
Used in Household Cleaning Products:
N-Chloro-p-benzoquinoneimine is used as a bleach and deodorizer in household cleaning products, helping to remove stains and eliminate odors.
It is important to handle N-Chloro-p-benzoquinoneimine with care due to its potential to cause irritation to the skin, eyes, and respiratory system, and its harmful effects if ingested or inhaled in large amounts.

InChI:InChI=1/C6H4ClNO/c7-8-5-1-3-6(9)4-2-5/h1-4H

Upstream product

• 123-30-8 4-amino-phenol 
• 62-53-3 aniline 
• 637-62-7 p-benzoquinone oxime 
• 1079-66-9 chloro-diphenylphosphine 
• 51-78-5 p-aminophenol hydrochloride 
• 7664-41-7 ammonia 
• 7732-18-5 water 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 106-51-4 p-benzoquinone 
• 7647-01-0 hydrogenchloride 
• 589-57-1 diethyl phosphorylchloridite 

Downstream Products

• 109567-37-5 4-(8-acetoxy-[5]quinolylimino)-cyclohexa-2,5-dienone 
• 30128-02-0 2,6-dimethyl-[1,4]benzoquinone-4-(4-hydroxy-phenylimine) 
• 109565-36-8 [1,4]benzoquinone-mono-(4-acetoxy-[1]naphthylimine) 
• 74129-09-2 bromo-[1,4]benzoquinone-1-(4-hydroxy-phenylimine) 
• 101821-22-1 2-isopropyl-5-methyl-[1,4]benzoquinone-1-(4-hydroxy-phenylimine) 
• 74098-31-0 chloro-[1,4]benzoquinone-4-(4-hydroxy-phenylimine) 
• 500-85-6 indophenol 
• 859771-41-8 [1,4]benzoquinone-mono-(4-hydroxy-3-methoxy-phenylimine) 
• 2582-31-2 [1,4]benzoquinone-mono-(4-hydroxy-2-methyl-phenylimine) 
• 2835-04-3 5-amino-2-hydroxybenzenesulfonic acid 
• 41772-21-8 N-phenylthio-1,4-benzoquinone imine 
• 30128-00-8 methyl-[1,4]benzoquinone-1-(4-hydroxy-phenylimine) 
• 30127-99-2 methyl-[1,4]benzoquinone-4-(4-hydroxy-phenylimine) 
• 6201-64-5 [1,4]benzoquinone-mono-(4-anilino-phenylimine) 

Relevant academic research and scientific papers

Semi-empirical MO-calculations on the electronic spectra of benzoquinonechlorimides

The electronic spectra of chloro p-benzoquinone(4)-chlorimides have been studied and the energy levels have been calculated using PPP-CI procedure, on the basis of which, the spectral bands have been assigned.The results show that the p-benzoquinone(4)-chlorimide possesses a n-?* transition at 23.25 kk and three ?-?* transitions, one strongly allowed at 35.46 kk and two weakly allowed at 44.44 and 30.30 kk.Substitution by chlorine atom in the quinonoid ring does not change the spectral pattern appreciably.A comparison of the spectrum of p-benzoquinone with those of its mono and dichlorimide clearly reveals that the strongly allowed ?-?* transition and the lowest weakly allowed ?-?* transition shift bathochromically and the ?-?* transition hypsochromically as the oxygen atoms in p-benzoquinone are replaced progressively by chlorimino groups.An additional weakly allowed ?-?* transition is found around 44.44 kk in quinonechlorimides.Inversion is shown to result in allowedness of transition from HOMO to LVMO in quinonechlorimides whereas it is forbidden in the case of quinones.