76049-50-8

Basic information

• Product Name: (5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone
• Synonyms: (5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone
• CAS NO: 76049-50-8
• Molecular Formula: C₁₃H₇Cl₂IO
• Molecular Weight: 377.00455
• Product Categories: pharmacetical
• Mol File: 76049-50-8.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone(76049-50-8)
• EPA Substance Registry System: (5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone(76049-50-8)

Safety Data

• Hazardous Substances Data: 76049-50-8(Hazardous Substances Data)

Usage

Description

(5-Chloro-2-iodophenyl)-(2-chlorophenyl)-methanone is a chemical compound with the molecular formula C13H8Cl2IO. It is a ketone derivative that contains both iodine and chlorine atoms, giving it a unique and potentially valuable chemical structure.

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

• 635-21-2 5-chloroanthranilic acid 
• 4743-17-3 5-Chloroisatoic anhydride 
• 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

• 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 
• 78367-91-6 2-<<4-chloro-2-(2-chlorobenzoyl)phenyl>-3-oxopropyl>-1H-isoindole-1,3(2H)-dione 
• 81389-13-1 2-<<5-chloro-3-(2-chlorophenyl)-1-oxo-1H-inden-2-yl>methyl>-1H-isoindole-1,3(2H)-dione 
• 81389-18-6 3-<(methanesulfonyl)oxy>-1-<4-chloro-2-(2-chlorobenzoyl)phenyl>propyne 
• 81389-15-3 8-chloro-9b-(2-chlorophenyl)-3,4-dihydro-9aH-oxazirino<3,2-a><2>benzazepin-5-(5H)-one 
• 81389-23-3 8-chloro-1-(2-chlorophenyl)-4-(1-pyrrolidinyl)-3H-2-benzazepine 
• 76049-78-0 8-chloro-1-(2-chlorophenyl)-3,4-dihydro-5H-2-benzazepin-5-one 2-oxide 

Relevant articles and documents

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.

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

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