CAS 7751-38-4
:Dichloro(diisopropyl)silane
Description :
Dichloro(diisopropyl)silane est un composé organosiliconé caractérisé par sa formule chimique C6H14Cl2Si. Il présente un atome de silicium lié à deux groupes isopropyles et deux atomes de chlore. Ce composé est typiquement un liquide incolore à jaune pâle avec une odeur distinctive. Il est connu pour sa réactivité, en particulier lors de l'hydrolyse, où il peut réagir avec l'eau pour produire du silanol et de l'acide chlorhydrique. Dichloro(diisopropyl)silane est principalement utilisé dans la synthèse de polymères de silicone et comme agent de couplage dans divers processus chimiques. Il est important de manipuler cette substance avec précaution, car elle peut être corrosive et présente des risques pour la santé en cas d'exposition. Des mesures de sécurité appropriées, y compris l'utilisation d'équipements de protection individuelle et une ventilation adéquate, sont essentielles lors de la manipulation de ce produit chimique. De plus, il est classé comme matériau dangereux, nécessitant le respect des réglementations pertinentes pour le stockage et l'élimination.
Formule :C6H14Cl2Si
InChI :InChI=1/C6H14Cl2Si/c1-5(2)9(7,8)6(3)4/h5-6H,1-4H3
SMILES :CC(C)[Si](C(C)C)(Cl)Cl
Synonymes :- Dichlorodiisopropylsilane
- Dichloro[Bis(1-Methylethyl)]Silane
Trier par
Degré de pureté (%)
0
100
|
0
|
50
|
90
|
95
|
100
6 produits concernés.
Dichlorodiisopropylsilane
CAS :Formule :C6H14Cl2SiDegré de pureté :>98.0%(GC)Couleur et forme :Colorless to Light yellow to Light orange clear liquidMasse moléculaire :185.16Dichlorodiisopropylsilane
CAS :Formule :C6H14Cl2SiDegré de pureté :98%Couleur et forme :LiquidMasse moléculaire :185.1669Dichlorodiisopropylsilane
CAS :DichlorodiisopropylsilaneDegré de pureté :95%Masse moléculaire :185.17g/molDiisopropyldichlorosilane
CAS :<p>S06800 - Diisopropyldichlorosilane</p>Formule :C6H14Cl2SiDegré de pureté :>98.0%(GC)Couleur et forme :LiquidMasse moléculaire :185.16000366210938DIISOPROPYLDICHLOROSILANE
CAS :<p>Bridging Silicon-Based 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>Alkyl Silane - Conventional Surface Bonding<br>Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure.<br>Diisopropyldichlorosilane; Dichlorobis(1-methylethyl)silane; DIPS<br>Forms bis(blocked) or tethered alcoholsUsed as tether in ring-closing-metathesis (RCM) reactionThe bifunctional nature of the reagent allows for the templating of diverse groups in intermolecular reactions and ring formationProtects 3’,5’ hydroxyls of nucleosides, but less effectively than SIT7273.0Forms tethered silyl ethers from diolsSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure<br></p>Formule :C6H14Cl2SiCouleur et forme :Straw Amber LiquidMasse moléculaire :185.17Dichlorodiisopropylsilane
CAS :<p>Dichlorodiisopropylsilane is a cycloaddition process, which is the addition of two molecules to create a new ring. It reacts with an unsaturated organic compound, such as an alkene or alkyne, to produce a reactive functional group. Dichlorodiisopropylsilane has been used in chemistry as a cross-linking agent for proteins and as a solid catalyst. The chemical stability of dichlorodiisopropylsilane makes it useful in the synthesis of model proteins. This compound also has low bioavailability due to its high reactivity with hydrochloric acid found in the stomach.</p>Formule :C6H14Cl2SiDegré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :185.17 g/mol





