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

Description

Silane, [(2-iodophenyl)ethynyl]trimethylis a chemical compound that consists of a silicon atom bonded to three methyl groups and one ethynyl group attached to a phenyl ring with an iodine atom. It is recognized for its high reactivity and ability to react with a broad spectrum of functional groups, making it a valuable tool in the synthesis of complex organic molecules and polymers. This versatile chemical building block is also utilized as a precursor in the preparation of various functionalized silanes, which find applications in materials science, pharmaceuticals, and other industries.

Uses

Used in Organic and Polymer Chemistry:
Silane, [(2-iodophenyl)ethynyl]trimethylis used as a reagent in organic and polymer chemistry for its high reactivity and ability to react with a wide range of functional groups. This makes it instrumental in the synthesis of complex organic molecules and polymers, contributing to the development of new materials and compounds.
Used in Materials Science:
In the field of materials science, Silane, [(2-iodophenyl)ethynyl]trimethylis used as a precursor in the preparation of functionalized silanes. These silanes are essential in creating advanced materials with specific properties tailored for various applications, such as coatings, adhesives, and sealants.
Used in Pharmaceutical Industry:
The pharmaceutical industry also benefits from Silane, [(2-iodophenyl)ethynyl]trimethylas a precursor for functionalized silanes. These silanes can be incorporated into drug molecules to enhance their properties, such as solubility, stability, and bioavailability, leading to improved therapeutic effects.
Overall, Silane, [(2-iodophenyl)ethynyl]trimethylis a crucial component in the development of innovative products and materials across multiple industries, thanks to its unique structure and reactivity.

Upstream product

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

Downstream Products

• 305350-73-6 1,4-Bis-(2-trimethylsilanylethynyl-phenylethynyl)-2-undecyloxy-benzene 
• 305350-74-7 11-[2,5-bis-(2-trimethylsilanylethynyl-phenylethynyl)-phenoxy]-undecanoic acid methyl ester 
• 897655-85-5 1,3-Dibromo-2-(2-ethynyl-phenylethynyl)-benzene 
• 897655-87-7 1,3-Dibromo-2-[2-(4,4-dimethyl-3-phenyl-pent-1-ynyl)-phenylethynyl]-benzene 
• 897655-94-6 1-[2-(2,6-dibromo-phenylethynyl)-phenylethynyl]-2,2-dimethyl-indan 
• 897655-86-6 α-[[2-[(2,6-dibromophenyl)ethynyl]phenyl]ethynyl]-α-(1,1-dimethylethyl)benzenemethanol 
• 897655-93-5 1-[2-(2,6-dibromo-phenylethynyl)-phenylethynyl]-2,2-dimethyl-1,2,3,4-tetrahydro-naphthalene 
• 909022-86-2 2-(2-(ethynylphenyl)ethynyl)-2'-methoxy-1,1'-binaphthyl 
• 897655-92-4 1-[[2-[(2,6-dibromophenyl)ethynyl]phenyl]ethynyl]-2,3-dihydro-2,2-dimethyl-1H-inden-1-ol 
• 897655-91-3 1-[[2-[(2,6-dibromophenyl)ethynyl]phenyl]ethynyl]-1,2,3,4-tetrahydro-2,2-dimethyl-1-naphthalenol 
• 909022-88-4 2-[2-(4,4-dimethyl-3-phenyl-pent-1-ynyl)-phenylethynyl]-2'-methoxy-[1,1']binaphthalenyl 
• 909022-87-3 1-[2-(2'-methoxy-[1,1']binaphthalenyl-2-ylethynyl)-phenyl]-4,4-dimethyl-3-phenyl-pent-1-yn-3-ol 
• 213599-21-4 1-(2-bromoethynyl)-2-iodobenzene 

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

Toward Cove-Edged Low Band Gap Graphene Nanoribbons

Graphene nanoribbons (GNRs), defined as nanometer-wide strips of graphene, have attracted increasing attention as promising candidates for next-generation semiconductors. Here, we demonstrate a bottom-up strategy toward novel low band gap GNRs (Eg/s