606-10-0

Usage

Uses

Used in Manufacturing and Industrial Processes:
2,2'-Diaminobenzophenone is used as a chemical intermediate for the synthesis of various compounds and materials in the manufacturing and industrial sectors. Its aromatic amine structure makes it a valuable component in the production of dyes, pigments, and pharmaceuticals.
Used in Dye and Pigment Production:
2,2'-Diaminobenzophenone is used as a key ingredient in the production of dyes and pigments, contributing to their color and stability. Its chemical properties allow for the creation of a wide range of hues and shades, making it an essential component in the dye and pigment industry.
Used in Pharmaceutical Synthesis:
2,2'-Diaminobenzophenone is used as a building block in the synthesis of various pharmaceutical compounds. Its aromatic amine structure enables the formation of complex molecules with potential therapeutic applications, making it a valuable asset in the development of new drugs.
Used in Environmental Protection:
Despite its potential hazards, 2,2'-Diaminobenzophenone can also be used in the development of environmental protection measures. Its properties can be harnessed to create compounds that help in the remediation of contaminated sites or the reduction of environmental pollution, contributing to a cleaner and safer environment.

Upstream product

• 51727-42-5 2,2'-dinitro-benzophenone 
• 39070-69-4 phenyl (3-amino-4-nitrophenyl)-methanone 
• 615-43-0 2-iodophenylamine 

Downstream Products

• 94575-36-7 2,2'-bis-acetylamino-benzophenone 
• 260-94-6 acridine 
• 25187-02-4 o,o'-diiodobenzophenone 
• 578-95-0 10H-acridin-9-one 
• 107428-45-5 6-(2-chlorophenyl)-7-hydroxy-5,8-diazabenzophenanthrene 
• 132934-38-4 6-ethyl-7-methyl-5,8-diazabenzo[c]phenanthrene 
• 195-27-7 Benzo<3,6>phenanthrolin 
• 4694-51-3 6-Hydroxy-7-mrthyl-benzo(3,6)-phenanthrolin 
• 5002-81-3 10H,11H,12H-dihydroquino[2,3,4-kl]acridine 
• 100259-60-7 7,7-Dimethyl-7,8-dihydro-6H-dibenzophenanthrolin 
• 89382-22-9 6,7-Dimethyl-benzo<3,6>phenanthrolin 
• 90-47-1 xanth-9-one 
• 339155-46-3 3(N)-(2,2'-diaminobenzophenone)-5-hydroxy-1,4-naphthoquinone 
• 107428-41-1 6-chloro-7-(2-chlorophenyl)-5,8-diazabenzophenanthrene 

Relevant academic research and scientific papers

Synthesis and electrophilic substitution of pyrido[2,3,4-kl]-acridines

Several new pyrido[2,3,4-kl]acridines were synthesized by reacting naphthoquinone, juglone or cyclohexan-1,3-dione with β,β'- diaminoketones in a biomimetic reaction. The structure of all new compounds was elucidated by NMR and MS spectroscopy. Electrophi

Nickel catalyzed electrosynthesis of ketones from organic halides and metal carbonyls

Ketones can be easily obtained by electroreduction in an undivided cell of an organic halide-metal carbonyl mixture using a Ni-bpy catalytic system in DMF (bpy = 2,2'-bipyridine). The process is especially well convenient for primary benzyl and alkyl halides.

Antiviral benzimidazoles

Certain N-substituted benzimidazoles are disclosed. The compounds are potent antiviral agents. Pharmaceutical formulations containing such compounds and a method of treating viral infections are provided.

ELECTROCHEMICAL REDUCTION OF 2,2'-DINITRODIPHENYLMETHANE AND 2,2'-DINITROBENZOPHENONE AT MERCURY ELECTRODES

The last two compounds in a 5-membered series of aromatic dinitrocompounds are reduced in a completely different manner at mercury electrodes. 2,2'-Dinitrodiphenylmethane (I) - in which a conjugation of both symmetrical moieties is ruled out - is electrolytically reduced in an eight-electron step to a bishydroxylamine this being most stable between pH 4.5 and 5.0.In processing the catholyte increase in concentration of this product leads to its intermolecular disproportionation, resulting in the formation of dibenzo-1,2-diazepine 5-oxide (IV) and2,2'-diaminodiphenylmethane (III). 2,2'-Dinitrobenzophenone (II) reduces at more positive potentials.Its preparative electrolysis in acetonitrile (with 0.1M-N(n-C4H9)4PF6 as supporting electrolyte) the application of which was made necesarry by the low solubility of II in ethanol, proceeds in an anomalous way.In the most positive cathodic wave a radical anion results, the following cathodic wave corresponds to a 6-electron reduction of one nitro group to an amino group while the other nitro group splits off as the anion NO2(-) (this later giving an anodic wave).Its formation has been proved by standard addition in polarography and by a qualitative analytical test.The product which results through this electrode process and a follow-up chemical reaction is acridone.This is turn, reduces in the third, most negative 4-electron wave to dihydroacridine.The comparison of all substances studied in this series reveals that their reducibility decreases with respect to the link X, viz. in the sequence CO > O > S and CH2 > NH.The electrolytical reduction on mercury cathodes occurs in a similar manner with analogues where X=O, S or CH2.Here, the main intermediate is the bis-hydroxylamine the stability of which predetermines the structure of final products.The other group comprises the substances with X=CO and NH.Here the main intermediate is the 2-nitro-2'-amino-diphenyl-X which is formed in a 6-electron process taking place at one of the nitro groups.The follow-up cyclization reaction leading to seven-membered heterocyclic rings located between two benzene nuclei only occurs with analogues of the type X=CH2, O and S.A partial reduction of dinitro compounds of this series has been observed with the analogue containing the NH link although that with X=CO has generally good preconditions for this mechanism.