76049-50-8

Usage

Uses

Used in Organic Synthesis:
(5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure, which includes both iodine and chlorine atoms, may provide novel reactivity and properties that can be exploited in the synthesis of complex molecules.
Used in Pharmaceutical Research:
(5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone is used as a research compound in the pharmaceutical industry. Its potential reactivity and unique properties may make it a valuable tool in the development of new drugs and therapeutic agents. However, further research is needed to fully understand its potential applications and limitations in this field.
Used in Chemical Industry:
(5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone may also find applications in the chemical industry, where its unique structure could be utilized in the production of specialty chemicals or materials with specific properties. (5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone's potential reactivity and the presence of both iodine and chlorine atoms may offer new opportunities for chemical innovation and development.
Safety Note:
As with all chemicals, (5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone should be handled with care and caution due to potential hazards associated with its use and storage. Proper safety measures, including the use of personal protective equipment and adherence to established safety protocols, should be followed to minimize risks.

Upstream product

• 4743-17-3 5-Chloroisatoic anhydride 
• 635-21-2 5-chloroanthranilic acid 
• 694-80-4 2-bromo-1-chlorobenzene 
• 150879-48-4 N-methyl-N-methyloxy-2-amino-5-chlorobenzamide 
• 2958-36-3 (2-amino-5-chloro-phenyl)-(2-chloro-phenyl)-methanone 

Downstream Products

• 76049-54-2 N-<<4-chloro-2-(2-chlorobenzoyl)phenyl>-3-propynyl>isoindole-1,3(2H)-dione 
• 87999-64-2 2',5-Dichloro-2-(5-cyano-4-pyrimidinyl)benzophenone 
• 3096-47-7 2-chloro-9H-fluoren-9-one 
• 87999-62-0 5,5'-Dimethyl-4,4'-bipyrimidinyl 
• 87999-60-8 2',5-Dichloro-2-(5-methyl-4-pyrimidinyl)benzophenone 
• 87999-61-9 2,2'-Bis(o-chlorobenzoyl)-4,4'-dichlorobiphenyl 
• 81389-17-5 3-hydroxy-1-<4-chloro-2-(2-chlorobenzoyl)phenyl>propyne 
• 81389-26-6 8-chloro-1-(2-chlorophenyl)-3,5-dihydrospiro<4H-2-benzazepine-4,2'-<1,3>dithiolane> 
• 81389-19-7 3-(hydroxyamino)-1-<4-chloro-2-(2-chlorobenzoyl)phenyl>propyne 
• 76049-70-2 8-chloro-1-(2-chlorophenyl)-3,4-dihydro-5H-2-benzazepin-5-one 
• 76049-71-3 methanesulfonate of 8-chloro-3,4-dihydro-1-(2-chlorophenyl)-5H-2-benzazepin-5-one 
• 81389-14-2 2-<<5-chloro-3-(2-chlorophenyl)-2,3-dihydro-3-hydroxy-1-oxo-1H-inden-2-yl>methyl>-1H-isoindole-1,3(2H)-dione 
• 81389-12-0 2-<1-<6-chloro-4-(2-chlorophenyl)-1-phthalazinyl>ethyl>-1H-isoindole-1,3(2H)-dione 
• 81389-21-1 2-<3-<4-chloro-2-(2-chlorobenzoyl)phenyl>-2-oxopropyl>-1H-isoindole-1,3(2H)-dione 

Relevant academic research and scientific papers

Synthesis of Diiodinated All-Carbon 3,3′-Diphenyl-1,1′-spirobiindene Derivatives via Cascade Enyne Cyclization and Electrophilic Aromatic Substitution

A synthetic method for the construction of diiodinated all-carbon spirobiindene derivatives has been developed from the reaction of propargyl alcohol-tethered alkylidenecyclopropanes with iodine. The reaction proceeded through an iodination-initiated cascade intramolecular enyne cyclization and electrophilic aromatic substitution reaction process in 1,2-dichloroethane upon heating, giving desired spirocyclic products in moderate to excellent yields. Further transformation of the obtained products has also been presented.

Cu(I)-Catalyzed Coupling and Cycloisomerization of Diazo Compounds with Terminal Yne-Alkylidenecyclopropanes: Synthesis of Functionalized Cyclopenta[ b]naphthalene Derivatives

A Cu(I)-catalyzed coupling and cycloisomerization of diazo compounds with terminal yne-alkylidenecyclopropanes (ACPs) has been presented. This reaction starts from the formation of an allenic intermediate in the Cu(I)-catalyzed cross-coupling reaction of a diazo compound with terminal alkyne in yne-tethered ACP and then undergoes a domino cycloisomerization of a 6π-electrocyclization and cyclopropane ring-opening rearrangement to give functionalized cyclopenta[b]naphthalene derivatives in moderate to excellent yields under mild conditions.

Compounds and methods for inhibiting mitotic progression

This invention relates to compounds and methods for the treatment of cancer. In particular, the invention provides compounds that inhibit Aurora kinase, pharmaceutical compositions comprising the compounds, and methods of using the compounds for the treat

3H-2-Benzazepines

There is presented 3H-2-benzazepines and 4,5-dihydro-3H-2-benzazepines of the formula STR1 wherein X is hydrogen, chloro or bromo, Y is hydrogen, fluoro or chloro with the proviso that X and Y cannot both be hydrogen and R1 is selected from the

Pyrimido[4,5-d][2]benzazepines

There is presented a compound of the formula STR1 wherein R1 is selected from the group consisting of hydrogen, lower alkyl, chloro, bromo, alkoxy, hydroxy, lower alkyl substituted thio and NR4 R5 wherein R4 and

2-Benzazepines. 1. Synthesis of 2-Benzazepin-4-ones and -5-ones via 2-Acetylenic Benzophenones

The preparation of 1-phenyl-2-benzazepin-4-ones and -5-ones is discussed.The palladium-catalyzed coupling of an iodobenzophenone to a monosubstituted acetylene assembles the necessary atoms required for the benzazepine ring.Transformation of the acetylene

Intermediates in the production of 2-benzazepines

Compounds of the formula STR1 wherein X and Y are selected from the group consisting of hydrogen, halogen and trifluoromethyl, are disclosed. The compounds are useful as intermediates in the production of 2-benzazepines, compounds of pharmacological activ

Triazolobenzazepines and processes for their production

There is presented triazolobenzazepines of the formula STR1 wherein R1 is hydrogen or lower alkyl and X and Y are hydrogen or halogen and the pharmaceutically acceptable salts thereof. Also disclosed are novel processes and intermediates leadin