CAS 58479-61-1
:cloruro de tert-butilfenilsililo
Descripción:
cloruro de tert-butilfenilsililo, con el número CAS 58479-61-1, es un compuesto organosilícico caracterizado por la presencia de un grupo tert-butilo y dos grupos fenilo unidos a un átomo de silicio, junto con un grupo funcional cloruro. Este compuesto típicamente aparece como un líquido incoloro a amarillo pálido y es conocido por su reactividad, particularmente como un agente silylante en la síntesis orgánica. Se utiliza comúnmente para proteger grupos hidroxilo en alcoholes y fenoles durante varias reacciones químicas, facilitando la formación de éteres silyl. La presencia del voluminoso grupo tert-butilo imparte hindrance estérica, lo que puede influir en la selectividad y reactividad del compuesto en aplicaciones sintéticas. Además, cloruro de tert-butilfenilsililo es sensible a la humedad y debe ser manejado en condiciones anhidras para prevenir la hidrólisis, que puede llevar a la formación de subproductos no deseados. En general, su estructura única y reactividad lo convierten en una herramienta valiosa en el campo de la química orgánica, particularmente en la síntesis de moléculas complejas.
Fórmula:C16H19ClSi
InChI:InChI=1S/C16H19ClSi/c1-16(2,3)18(17,14-10-6-4-7-11-14)15-12-8-5-9-13-15/h4-13H,1-3H3
Clave InChI:InChIKey=MHYGQXWCZAYSLJ-UHFFFAOYSA-N
SMILES:[Si](C(C)(C)C)(Cl)(C1=CC=CC=C1)C2=CC=CC=C2
Sinónimos:- (1,1-Dimethylethyl)diphenylsilyl chloride
- (Chloro)(tert-butyl)diphenylsilane
- 1,1′-[Chloro(1,1-dimethylethyl)silylene]bis[benzene]
- Benzene, 1,1'-[chloro(1,1-dimethylethyl)silylene]bis-
- Chloro(1,1-dimethylethyl)diphenylsilane
- Chlorodiphenyl-tert-butylsilane
- Diphenyl-tert-butylsilyl chloride
- Nsc 617386
- Silane, Tert-Butyl-Diphenylchloro-
- TBDPSCl
- TDBPSCl
- Terc-Butilclorodifenilsilano
- t-Butylchlorodiphenylsilane
- t-Butyldiphenylchlorosilane
- tert-Butylchlordiphenylsilan
- tert-Butylchlorodiphenylsilane
- tert-Butyldiphenylchlorosilane
- tert-Butyldiphenylsilyl chloride
- Ver más sinónimos
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Encontrado 7 productos.
tert-Butyldiphenylchlorosilane
CAS:Fórmula:C16H19ClSiPureza:>97.0%(GC)Forma y color:Colorless to Light orange to Yellow clear liquidPeso molecular:274.86tert-Butyldiphenylchlorosilane, 97%
CAS:<p>tert-Butyldiphenylchlorosilane acts as a silylating reagent used to protect alcohols and in the preparation of silyl ethers. It plays a major role as a raw material and a precursor in organic synthesis and pharmaceuticals. It is also used for the synthesis of interphenylene phenyloxazoles which can </p>Fórmula:C16H19ClSiPureza:97%Forma y color:Liquid, Clear colorless to yellow or pinkPeso molecular:274.86tert-Butyldiphenylchlorosilane
CAS:Fórmula:C16H19ClSiPureza:98%Forma y color:LiquidPeso molecular:274.8606Ref: IN-DA0035NJ
5g20,00€1kg184,00€25g28,00€50g40,00€5kgA consultar100g55,00€10kgA consultar250g96,00€500g143,00€4x1kg857,00€(tert-Butyl)(chloro)diphenylsilane
CAS:(tert-Butyl)(chloro)diphenylsilaneFórmula:C16H19ClSiPureza:≥95%Forma y color: clear. light orange liquidPeso molecular:274.86056g/moltert-Butyldiphenylchlorosilane
CAS:Producto controlado<p>Applications tert-Butyldiphenylchlorosilane is used to synthesize interphenylene phenyloxazoles, compounds that have antagonistic activity against thromboxane receptors which can be used for treatment of circulatory disorders, angina and stroke.<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 Hadjipavlou–Litina, D. & Kontogiorgis, C.: Int. Elect. J. Mol. Des., 1, 300 (2002); Misra, R., et al.: Bioorg. Med. Chem. Lett., 2, 937 (1992)<br></p>Fórmula:C16H19ClSiForma y color:NeatPeso molecular:274.86tert-Butyl diphenylchlorosilane
CAS:<p>Tert-butyl diphenylchlorosilane is a chemical compound that belongs to the group of organosilicon compounds. It is used for the preparation of various organosilicon compounds, such as trifluoroacetic acid, which is used in analytical chemistry. The synthesis of tert-butyl diphenylchlorosilane starts with the reaction between hydrochloric acid and sodium citrate. This yields a phosphate bond and a hydroxyl group. In order to form the desired product, tert-butyl diphenylchlorosilane, this intermediate is reacted with trifluoroacetic acid in an asymmetric synthesis to yield the desired product. The reaction mechanism of this process involves hydrogen chloride as an electrophile attacking the carbonyl carbon atom in trifluoroacetic acid, leading to an elimination reaction. This elimination reaction results in two possible products: tert-butyl acetate or tert-butyl chloros</p>Fórmula:C16H19ClSiPureza:Min. 97 Area-%Forma y color:Clear LiquidPeso molecular:274.87 g/moltert-Butylchlorodiphenylsilane (TBDPSCl) extrapure AR, 98%
CAS:Fórmula:C16H19ClSiPureza:min. 98%Forma y color:Clear, Colourless to slight yellow, LiquidPeso molecular:274.86






