137648-47-6

Basic information

• Product Name: Silane, [(2-iodophenyl)ethynyl]trimethyl-
• CAS NO: 137648-47-6
• Molecular Formula: C11H13ISi
• Molecular Weight: 300.214
• Mol File: 137648-47-6.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: Silane, [(2-iodophenyl)ethynyl]trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, [(2-iodophenyl)ethynyl]trimethyl-(137648-47-6)
• EPA Substance Registry System: Silane, [(2-iodophenyl)ethynyl]trimethyl-(137648-47-6)

Safety Data

• Hazardous Substances Data: 137648-47-6(Hazardous Substances Data)

Usage

General Description

Silane, [(2-iodophenyl)ethynyl]trimethyl- is a chemical compound composed of a silicon atom bonded to three methyl groups and one ethynyl group that is in turn attached to a phenyl ring with an iodine atom. Silane, [(2-iodophenyl)ethynyl]trimethyl- is commonly used as a reagent in various organic and polymer chemistry reactions. It is known for its ability to react with a wide range of functional groups, and its high reactivity makes it a valuable tool in the synthesis of complex organic molecules and polymers. It is also used as a precursor in the preparation of various functionalized silanes, which have applications in materials science, pharmaceuticals, and other industries. Overall, Silane, [(2-iodophenyl)ethynyl]trimethyl- is an important chemical building block with versatile applications in diverse fields.

Upstream product

• 615-42-9 1,2-Diiodobenzene 
• 1066-54-2 trimethylsilylacetylene 
• 103529-16-4 2-[(trimethylsilyl)ethynyl]aniline 
• 265670-90-4 3,3-diethyl-1-(2-((trimethylsilyl)ethynyl)phenyl)triaz-1-ene 
• 38274-16-7 2-bromo-1-(trimethylsilylethynyl)benzene 
• 615-43-0 2-iodophenylamine 
• 265671-00-9 3,3-diethyl-1-(2-iodophenyl)triaz-1-ene 
• 129112-26-1 2-iodophenyltrifluoromethanesulfonic acid 
• 583-55-1 1-Bromo-2-iodobenzene 

Downstream Products

• 349659-52-5 2-chloro-5-[(2-trimethylsilylethynylphenyl)ethynyl]pyridine 
• 1163301-97-0 2,2'-(buta-1,3-diyne-1,4-diyl)bis[(3-hydroxypropynyl)benzene] 
• 155587-93-2 1,4-bis(2-iodophenyl)buta-1,3-diyne 
• 501371-01-3 6,6'-bis[(2-trimethylsilylethynylphenyl)ethynyl]-2,2'-bipyridine 
• 375366-58-8 4,16-bis(2'-(trimethylsilylethynyl)phenylethynyl)[2.2]paracyclophane 
• 305350-74-7 11-[2,5-bis-(2-trimethylsilanylethynyl-phenylethynyl)-phenoxy]-undecanoic acid methyl ester 
• 305350-73-6 1,4-Bis-(2-trimethylsilanylethynyl-phenylethynyl)-2-undecyloxy-benzene 
• 265670-92-6 C₂₃H₂₇N₃Si 
• 766-50-7 (2-iodophenyl)-acetylene 

Relevant articles and documents

Halogen Bonding Helicates Encompassing Iodonium Cations

The first halonium-ion-based helices were designed and synthesized using oligo-aryl/pyridylene-ethynylene backbones that fold around reactive iodonium ions. Halogen bonding interactions stabilize the iodonium ions within the helices. Remarkably, the distance between two iodonium ions within a helix is shorter than the sum of their van der Waals radii. The helical conformations were characterized by X-ray crystallography in the solid state, by NMR spectroscopy in solution and corroborated by DFT calculations. The helical complexes possess potential synthetic utility, as demonstrated by their ability to induce iodocyclization of 4-penten-1-ol.

Reversible Multicomponent and Gate Triggered by Stoichiometric Chemical Pulses Commands the Self-Assembly and Actuation of Catalytic Machinery

The present work demonstrates the operation of a reversible supramolecular gate, i.e., an ensemble of various components linked by chemical communication, which is triggered by stoichiometric chemical inputs and by obeying the AND truth table delivers a s

Synthesis of a carbon analogue of scytonemin

The synthesis of a carbon analogue of scytonemin was accomplished on the basis of molybdenum-mediated intramolecular double Pauson-Khand type reaction of bis(allenyne), followed by the double aldol condensation of the formed double Pauson-Khand type adduct.