155259-28-2

Basic information

• Product Name: 1,2-DIIODO-4,5-(DIDECYLOXY)BENZENE
• Synonyms: 1,2-DIIODO-4,5-(DIDECYLOXY)BENZENE
• CAS NO: 155259-28-2
• Molecular Formula: C₂₆H₄₄I₂O₂
• Molecular Weight: 642.44
• Mol File: 155259-28-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-DIIODO-4,5-(DIDECYLOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DIIODO-4,5-(DIDECYLOXY)BENZENE(155259-28-2)
• EPA Substance Registry System: 1,2-DIIODO-4,5-(DIDECYLOXY)BENZENE(155259-28-2)

Safety Data

• Hazardous Substances Data: 155259-28-2(Hazardous Substances Data)

Usage

Chemical structure

Diiodinated benzene derivative
The benzene ring has two iodine atoms attached to the 1 and 2 positions.

Substituents

Two decyloxy groups on the 4 and 5 positions
Decyloxy groups are alkyl chains with 10 carbon atoms, attached to the benzene ring through an oxygen atom.

Applications

Organic synthesis, chemical research
Used as a reagent or building block for the synthesis of more complex organic molecules.

Industries

Pharmaceutical, agrochemical, and material science
Potential applications in these industries due to its unique chemical structure and properties.

Research value

Investigating structure-activity relationships, developing new chemical reactions
Its unique structure makes it a valuable tool for understanding and creating new chemical reactions.

Safety precautions

Handle with care, use proper safety guidelines
Due to its chemical reactivity and potential health hazards, it should be handled and used with caution and in accordance with established safety guidelines.

Upstream product

• 112-29-8 1-bromo dodecane 
• 2050-77-3 Iododecane 
• 120-80-9 benzene-1,2-diol 
• 25934-47-8 1,2-bis-decyloxy-benzene 

Downstream Products

• 155259-29-3 1,2-bis(decyloxy)-4,5-diethynylbenzene 
• 118132-12-0 4,5-dicyano-1,2-bis-(decyloxy)benzene 
• 1196205-95-4 1,2-didecyloxy-4,5-bis[1-(3-hydroxy-3-methyl-1-butynyl)]benzene 
• 1155876-58-6 C₆₂H₉₄I₂O₄S₄ 
• 862259-95-8 [2-(2,5-bis-decyloxy-4-ethynyl-phenylethynyl)-4,5-bis-decyloxy-phenylethynyl]-triisopropyl-silane 
• 862259-93-6 1,2-bis(decyloxy)-4-trisiopropylsilylethynyl-5-trimethylsilylethynylbenzene 
• 862259-94-7 1,2-bis(decyloxy)-4-ethynyl-5-trisiopropylsilylethynylbenzene 
• 252935-59-4 1,2-bis(decyloxy)-4-ethynyl-5-iodobenzene 
• 862259-92-5 1,2-bis(decyloxy)-4-iodo-5-(trimethylsilyl)ethynylbenzene 

Relevant articles and documents

Effect of phthalimide in 2,1,3-benzooxadiazole based copolymer on the performances of solar cells

Two newly designed donor-acceptor (D-A) conjugated polymers were prepared from the Stille coupling reactions by incorporating phthalimide derivative as a co-acceptor unit into 2,1,3-benzooxadiazole (BO) and thiophene with different ratios of 5 mol.% and 1

Two-dimensional porous molecular networks of dehydrobenzo[12]annulene derivatives via alkyl chain interdigitation

The self-assembly of a series of hexadehydrotribenzo[12]annulene (DBA) derivatives has been scrutinized by scanning tunneling microscopy (STM) at the liquid-solid interface. First, the influence of core symmetry on the network structure was investigated b

Synthesis of Diacetylene Macrocycles Derived from 1,2-Diethynylbenzene Derivatives: Structure and Reactivity of the Strained Cyclic Dimer

Diacetylene macrocycles 2-4 (n=1-3) (R=H, C4H9, C6H13, C10H21, C12H25, OC10H21) have been prepared from the oxidative coupling of 1,2-diethynylbenzene derivatives.These compounds can be produced in useful quantities and are of interest as precursors to novel conjugated organic polymers.The reported results indicate that when the R groups are large the dimeric macrocycle (n=1) can be prepared in as high as 74percent yield from the corresponding 1,2-diethynylbenzene in a one-step procedure.An alternate multistep procedure was found to produce the tetrameric macrocycle (n=3,R=C6H13) in 45percent yield.The highly strained dimeric macrocycle was characterized by an X-ray structure and was found to be very reactive.The dimers undergo a rapid very exothermic polymerization at 100-125 deg C, indicative of a chain reaction.Reaction of the dimeric macrocycles with iodine results in intramolecular cyclization and a new 20? electron tetraiodide fused ring system.Reaction of the tetraiodide with oxygen produces a related compound in which two of the iodides have been converted to ketones.