611182-95-7

Usage

Uses

Used in Organic Synthesis:
TIPS-OPh alcohol is utilized as a protecting group for alcohols in organic synthesis, providing a means to shield functional groups during chemical reactions, thus preventing unwanted side reactions and ensuring the desired product formation.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, TIPS-OPh alcohol is used as a precursor for the synthesis of complex organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, TIPS-OPh alcohol serves as a starting material for the creation of various compounds used in the development of pesticides, herbicides, and other agricultural chemicals.
Used in Material Science:
TIPS-OPh alcohol is also employed in material science for the synthesis of silicon-containing polymers and materials, which have potential applications in a range of fields due to their unique properties.
Used in Preparation of Silicon-Containing Materials:
As a useful reagent, TIPS-OPh alcohol is involved in the preparation of silicon-containing materials, which may have applications in areas such as electronics, where such materials can be used in the development of semiconductors or other components.

Upstream product

• 1085453-61-7 ethyl 4-(triisopropylsilyloxy)benzoate 
• 211617-68-4 4-(triisopropylsilyloxy)benzaldehyde 
• 13154-24-0 triisopropylsilyl chloride 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 123-08-0 4-hydroxy-benzaldehyde 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 20876-99-7 4-hydroxy-N,N-dimethyl-benzamide 

Downstream Products

• 611182-78-6 [4-(bromomethyl)phenoxy][tri(propan-2-yl)]silane 
• 1145732-90-6 (4-(iodomethyl)phenoxy)triisopropylsilane 
• 1609376-35-3 C₂₄H₃₈O₄Si 
• 1609376-36-4 C₂₄H₃₈O₄Si 
• 1609376-33-1 C₂₁H₂₉BrO₂Si 
• 1609376-34-2 C₂₄H₃₆O₂Si 
• 1609376-31-9 1-phenyl-5-(4-(triisopropylsilyloxy)benzylthio)-1H-tetrazole 
• 1085452-89-6 4-[(5-methyl-3-{3-[4-(trifluoromethoxy)phenyl]-1,2,4-oxadiazol-5-yl}-1H-pyrazol-1-yl)methyl]phenol 
• 1269415-94-2 diethyl (4-((triisopropylsilyl)oxy)benzyl)phosphonate 
• 1269171-09-6 C₃₃H₄₂N₂O₅Si 

Relevant academic research and scientific papers

Fluorescent probe for fluorine ion detection, application of fluorescent probe and method for detecting fluorine ions in to-be-detected sample

The invention belongs to the technical field of analytical chemistry, and particularly relates to a fluorescent probe for fluorine ion detection, application of the fluorescent probe and a method for detecting fluorine ions in a to-be-detected sample. The invention provides a compound as shown in a formula I, or an optical isomer or salt thereof, and provides application of the compound as a fluorine ion detection fluorescent probe. According to the method for detecting the fluorine ions in the to-be-detected sample, the compound, or the optical isomer or the salt of the compound is used as a fluorine ion detection fluorescent probe for detection. The fluorescent probe has the advantages of good water solubility, high selectivity, high response speed, low detection limit, good stability, wide applicable pH range and good application prospect.

NOVEL CARBONATE ANALOGUES BEARING PTEROSTILBENE AMINO ACIDS FOR THE TREATMENT OF NON-ALCOHOLIC FATTY LIVER DISEASE AND NON-ALCOHOLIC STEATOHEPATITIS

A series of novel analogs of water soluble pterostilbene amino acid bearing carbonates were synthesized, which show activities in treating a non-alcoholic fatty liver disease and a nonalcoholic steatohepatitis (NASH).

Controlled Reduction of Carboxamides to Alcohols or Amines by Zinc Hydrides

New protocols for controlled reduction of carboxamides to either alcohols or amines were established using a combination of sodium hydride (NaH) and zinc halides (ZnX2). Use of a different halide on ZnX2 dictates the selectivity, wherein the NaH-ZnI2 system delivers alcohols and NaH-ZnCl2 gives amines. Extensive mechanistic studies by experimental and theoretical approaches imply that polymeric zinc hydride (ZnH2)∞ is responsible for alcohol formation, whereas dimeric zinc chloride hydride (H?Zn?Cl)2 is the key species for the production of amines.

A fluoride activated methylene blue releasing platform for imaging and antimicrobial photodynamic therapy of human dental plaque

We report a F- activated methylene blue (MB) releasing platform for imaging and antimicrobial photodynamic therapy (aPDT). By utilizing this platform, one of the selected probes, FD-F3, displays a remarkable near-infrared fluorescence and absor

FLUORIDE FLUORESCENCE PROBE

Methylene blue (MB) derivatives selectively detect F? by desilylation reaction to act as a fluorescent probe.

METABOLICALLY ROBUST ANALOGS OF CYP-EICOSANOIDS FOR THE TREATMENT OF CARDIAC DISEASE

The present invention relates to compounds according to general formula (I) which are metabolically robust analogues of bioactive lipid mediators derived from omega-3 polyunsaturated fatty acids (n-3 PUFAs).The present invention further relates to composi

ANALOGS OF CYP-EICOSANOIDS FOR USE IN TREATING OR PREVENTING A DISORDER ASSOCIATED WITH NEOVASCULARIZATION AND/OR INFLAMMATION

The present invention relates to compounds according to general formula (I) which are metabolically robust analogues of bioactive lipid mediators derived from omega-3 polyunsaturated fatty acids (n-3 PUFAs) for use in treating or reducing the risk of deve

A Modular Access to (±)-Tubocurine and (±)-Curine - Formal Total Synthesis of Tubocurarine

Two consecutive Cu-catalyzed Ullmann-type C-O couplings permitted the first successful entry toward the curare alkaloids (±)-tubocurine and (±)-curine. Starting from vanillin, the synthetic sequence comprises 15 linear steps and includes a total of 24 transformations. In addition, the total synthesis of tubocurine represents a formal total synthesis of the famous arrow poison alkaloid tubocurarine.

Decarboxylative Csp3-Csp3 coupling for benzylation of unstable ketone enolates: Synthesis of: P -(acylethyl)phenols

A new decarboxylative Csp3-Csp3 coupling approach for the benzylation of ketone enolates has been developed. A variety of raspberry ketone derivatives were conveniently synthesized in good to excellent yields under mild conditions. A crossover reaction shed light on the mechanism of this tandem reaction.

Scalable asymmetric total syntheses of (+)-psoracorylifol B and (+)-ent-psoracorylifol C

The first, asymmetric total syntheses of potent antimicrobial Psoracorylifol B (>1.3 g obtained, dr 10.5:1) with a 9.4% overall yield on a gram scale in 14 steps and ent-Psoracorylifol C with a 4.3% yield in 16 steps were achieved. The key features of our synthesis include (i) sequential, rarely explored Achmatowicz rearrangement/bicycloketalization to construct the 6,8-dioxabicyclo[3.2.1]octane core, and (ii) Cu-mediated SN2′ methylation or Johnson-Claisen rearrangement to stereoselectively install the all-carbon quaternary stereocenter. This concise, highly efficient, and scalable synthetic route may provide expedited and practical access to psoracorylifols and their analogues for further biological activity evaluation.