7500-08-5

Basic information

• Product Name: 1-iodo-4-[(4-nitrophenyl)sulfanyl]benzene
• CAS NO: 7500-08-5
• Molecular Formula: C₁₂H₈INO₂S
• Molecular Weight: 357.1669
• Mol File: 7500-08-5.mol

Chemical Properties

• Boiling Point: 466.7°C at 760 mmHg
• Flash Point: 236.1°C
• Density: 1.82g/cm³
• Vapor Pressure: 1.93E-08mmHg at 25°C
• Refractive Index: 1.733
• CAS DataBase Reference: 1-iodo-4-[(4-nitrophenyl)sulfanyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-iodo-4-[(4-nitrophenyl)sulfanyl]benzene(7500-08-5)
• EPA Substance Registry System: 1-iodo-4-[(4-nitrophenyl)sulfanyl]benzene(7500-08-5)

Safety Data

• Hazardous Substances Data: 7500-08-5(Hazardous Substances Data)

Usage

Benzene derivative

A compound based on the benzene structure, which is a six-carbon ring with alternating single and double bonds.

Iodine atom

A halogen element present in the compound, which can influence the compound's reactivity, polarity, and solubility.

Nitrophenylsulfanyl group

A functional group consisting of a sulfur atom bonded to a 4-nitrophenyl group, which can impart specific chemical properties and reactivity.

Yellow to brown solid at room temperature

The compound's appearance and state, indicating its physical form and color under standard conditions.

Organic synthesis and pharmaceutical research

Common applications of the compound, which involve the creation of new organic compounds and the development of pharmaceuticals.

Reagent in chemical reactions

The compound's role as a reactant or catalyst in various chemical processes, facilitating the formation of new products.

Unique structure and properties

The compound's distinctive arrangement of atoms and its resulting characteristics, which can be valuable in the development of new compounds and materials.

Potential use in medicinal chemistry and drug discovery

The possibility that the compound may be useful in the design and development of new drugs due to its specific chemical properties and structure.

Upstream product

• 101-59-7 4-amino-4'-nitrodiphenyl sulfide 
• 21969-12-0 4-bromophenyl 4′-nitrophenyl sulfide 
• 106-53-6 para-bromobenzenethiol 
• 636-98-6 p-nitrobenzene iodide 

Downstream Products

• 59280-02-3 (4-iodo-phenyl)-(4-nitro-phenyl)-sulfone 
• 54952-19-1 1,4-bis(4-nitrophenylsulfenyl)benzene 
• 62248-52-6 4-Amino-4'-iod-diphenylsulfid 
• 865179-25-5 1-(4-nitrophenylthio)-4-(4-bromophenylthio)benzene 
• 874492-50-9 [4-(4-iodo-benzenesulfonyl)-phenyl]-[2]pyridyl-amine 
• 40915-23-9 4-(4-iodo-benzenesulfonyl)-aniline 
• 17619-11-3 1,4-bis(4'-aminophenylthio)benzene 
• 865179-31-3 1-(4-nitrophenylthio)phenylthio-4-(4-bromophenylthio)phenylthio-benzene 
• 865179-30-2 C₂₄H₁₆INO₂S₃ 
• 865179-29-9 ((4-nitrophenylthio)phenyl)((4-bromophenylthio)phenyl)thioether 
• 865179-27-7 I(C₆H₄S-4)2C₆H₄NO₂-4 

Relevant articles and documents

Synthesis of molecular chains: Application of cross-coupling and bromo by iodo exchange reactions

The synthesis of a series of molecular chains by use of C-S, C-N and C-Alkyne cross coupling, as well as bromo by iodo exchange reactions, has been reported. Two different types of chains R-C6H4-S-C6H4-CC-C6H4-NH-C6H4-Br, and R-C6H4-S-C6H4-NH-C6H4-CC-C6H4-Br (R=MeO, CN, NO2) could be obtained starting from the same thioether but applying different reaction sequences. Compounds R-C6H4-CC-C6H4-S-C6H4-NH-C6H4-Br were prepared from diaryl acetylenes after two bromo by iodo replacements alternated with a C-S and a C-N cross coupling.

A new approach to the synthesis of oligomers. Application to the synthesis of p-phenylene thioether wires

Oligothioethers 4-RC6H4(SC6H 4-4)nX (n = 1-3; X = Br, I; R = NO2; X = Br; R = MeO. n = 1 and 2; X = I; R = MeO. n = 4; X = Br; R = NO2) have been prepared through a process invol

Preparation of organic sulfone compounds

An in-situ process for preparing organic sulfone compounds by oxidizing the corresponding sulfide compound with a mixture of hydrogen peroxide, a carboxylic acid in the presence of a catalytic amount of a mineral acid or an organic sulfonic acid.