CAS 6485-79-6
:Triisopropylsilane
Description:
Triisopropylsilane, with the CAS number 6485-79-6, is an organosilicon compound characterized by its three isopropyl groups attached to a silicon atom. This compound is typically a colorless, volatile liquid with a distinctive odor. It is known for its low viscosity and relatively low boiling point compared to other silanes. Triisopropylsilane is often used as a reagent in organic synthesis, particularly in hydrosilylation reactions and as a protecting group for alcohols and amines due to its steric hindrance. Its chemical stability and non-reactivity under mild conditions make it a valuable compound in various chemical processes. Additionally, it exhibits hydrophobic properties, which can be advantageous in applications involving surface modification or in the formulation of silicone-based materials. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested. Overall, triisopropylsilane is a versatile compound with significant utility in both academic and industrial chemistry.
Formula:C9H22Si
InChI:InChI=1/C9H22Si/c1-7(2)10(8(3)4)9(5)6/h7-10H,1-6H3
InChI key:InChIKey=YDJXDYKQMRNUSA-UHFFFAOYSA-N
SMILES:[SiH](C(C)C)(C(C)C)C(C)C
Synonyms:- Silane, triisopropyl-
- Silane, tris(1-methylethyl)-
- Triisopropylhydrosilane
- Tripropan-2-Ylsilane
- Tris(1-methylethyl)silane
- Triisopropylsilane
- Tris-isopropylsilane
- SILANE IP3H
- Triisopropylsilane [Cas#
- (ME2CH)3SIH
- Triisopropylsilane ,97%
- TIS
- TIPS
- See more synonyms
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Found 8 products.
Triisopropylsilane
CAS:Formula:C9H22SiPurity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:158.36Triisopropylsilane, 98%
CAS:<p>Triisopropylsilane is used as a protecting group in peptide synthesis and is also used as a reducing agent for the selective reduction of anomeric C-phenyl ketals. It is used in the selective silylation of primary hydroxyl groups without affecting the secondary hydroxyl group. It is used in the prep</p>Formula:C9H22SiPurity:98%Color and Shape:Clear colorless, LiquidMolecular weight:158.36Triisopropylsilane
CAS:<p>Triisopropylsilane</p>Formula:C9H22SiPurity:98%Color and Shape: clear. colourless liquidMolecular weight:158.35647g/molTriisopropylsilane
CAS:<p>S17975 - Triisopropylsilane</p>Formula:C9H22SiPurity:98%Color and Shape:Clear LiquidMolecular weight:158.36Triisopropylsilane
CAS:Controlled Product<p>Applications Triisopropylsilane is used in the design of internalizing PSMA-specific Glu-ureido-based radiotherapeuticals for prostrate cancers. Reagent for the rational design of dual peptides targeting ghrelin and Y2 receptors to regulate food intake and body weight. Also functions as a highly selective reducing agent used in the preparation of anti-1,2-diols.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Wuestemann, T., et al.: Theranostics, 6, 1085 (2016); Kilian, T., et al.: J. Med. Chem., 58, 4180 (2015); Horners, L.; et al.: Organomet. Chem., 282, 155 (1985)<br></p>Formula:C9H22SiColor and Shape:NeatMolecular weight:158.36TRIISOPROPYLSILANE, 97%
CAS:<p>Trialkylsilyl Blocking Agent<br>Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.<br>Tri-substituted Silane Reducing Agent<br>Organosilanes are hydrocarbon-like and possess the ability to serve as both ionic and free-radical reducing agents. These reagents and their reaction by-products are safer and more easily handled and disposed than many other reducing agents. The metallic nature of silicon and its low electronegativity relative to hydrogen lead to polarization of the Si-H bond yielding a hydridic hydrogen and a milder reducing agent compared to aluminum-, boron-, and other metal-based hydrides. A summary of some key silane reductions are presented in Table 1 of the Silicon-Based Reducing Agents brochure.<br>Triisopropylsilane; Triisopropylsilylhydride; TIPS-H<br>Silylates strong acids with loss of hydrogenSilylates 1° alcohols selectivelySteric bulk allows for selective silylation of compounds with more than one hydroxyl groupSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochureVery sterically-hindered silaneBlocking agent forming derivatives stable in presence of Grignard reagentsSelectively silylates primary alcohols in presence of secondary alcoholsUsed as a cation scavenger in the deprotection of peptidesExtensive review of silicon based reducing agents: Larson, G.; Fry, J. L. "Ionic and Organometallic-Catalyzed Organosilane Reductions", Wipf, P., Ed.; Wiley, 2007<br></p>Formula:C9H22SiPurity:97%Color and Shape:LiquidMolecular weight:158.36Triisopropylsilane
CAS:<p>Triisopropylsilane is a water-soluble analog of trifluoroacetic acid. It is used in the synthesis of peptides and other organic compounds. Triisopropylsilane has been shown to have significant cytotoxicity against cancer cells, with a half maximal inhibitory concentration (IC) of 0.1 mM. This compound also has the ability to chelate transition metals and is used as a fluorescence probe for metal ions. The pharmacokinetics of triisopropylsilane are dependent on its sodium-dependent glucose uptake and hydroxyl group metabolism. Triisopropylsilane binds to DNA and RNA, inhibiting their synthesis, which may be related to its antiviral activity against HIV infections.</p>Formula:C9H22SiPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:158.36 g/mol
