CAS 1066-54-2
:(Trimetilsilil)acetileno
Descripción:
(Trimetilsilil)acetileno, con el número CAS 1066-54-2, es un compuesto organosilícico caracterizado por la presencia de un grupo trimetilsililo unido a una parte de acetileno. Este compuesto típicamente aparece como un líquido incoloro y es conocido por su volatilidad e inflamabilidad. Tiene una fórmula molecular de C5H10OSi, lo que indica la presencia de carbono, hidrógeno, oxígeno y silicio. El grupo trimetilsililo mejora la estabilidad de la estructura de acetileno, haciéndola menos reactiva que los acetilenos simples. (Trimetilsilil)acetileno se utiliza a menudo en la síntesis orgánica, particularmente en la formación de moléculas más complejas a través de reacciones como sustituciones nucleofílicas y reacciones de acoplamiento. Sus propiedades únicas le permiten servir como un grupo protector para alquinos terminales en diversas transformaciones químicas. Además, es soluble en disolventes orgánicos, lo que facilita su uso en diversas aplicaciones químicas. Se requieren precauciones de seguridad al manipular este compuesto debido a su naturaleza inflamable y los posibles riesgos para la salud asociados con la exposición.
Fórmula:C5H10Si
InChI:InChI=1S/C5H10Si/c1-5-6(2,3)4/h1H,2-4H3
Clave InChI:InChIKey=CWMFRHBXRUITQE-UHFFFAOYSA-N
SMILES:[Si](C#C)(C)(C)C
Sinónimos:- (Thrimethylsilyl)acetylene
- (Trimethylsilanyl)acetylene
- (Trimethylsilyl)acetylene
- 1-(Trimethylsilyl)acetylene
- 1-Trimethylsilylethyne
- 2,2-Dimethyl-2-sila-3-butyne
- Acetylene, Trimethylsilyl-
- Acetylenyltrimethylsilane
- Cetylene, Trimethylsilyl-
- Ethinyltrimethylsilane
- Ethynyltrimethylsilane
- Ilane, Ethynyltrimethyl-
- Ilane, Trimethyl-, Ethynyl-
- Ms Acetylene
- Rimethylethynylsilane
- Rimethylsilylacetylene,Min
- Silane, ethynyltrimethyl-
- TMS acetylene
- Thinyltrimethylsilane
- Thyne,-Trimethylsilyl
- Thynyltrimethyl-Silan
- Thynyltrimethylsilane
- Thynyltrimethylsilane, Wacker-Quality
- Timethylsilylacetylene
- Tmsa
- Trimethyl silyl acetylene
- Trimethylethynylsilane
- Trimethylsil yace tylene
- Trimethylsilanylethyne
- Trimethylsilyl)ethyne
- Trimethylsilylacetylen
- Trimethylsilylethyne
- Ver más sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 7 productos.
Trimethylsilylacetylene
CAS:Fórmula:C5H10SiPureza:>98.0%(GC)Forma y color:Colorless to Almost colorless clear liquidPeso molecular:98.22(Trimethylsilyl)acetylene, 98%
CAS:<p>(Trimethylsilyl)acetylene is used in the preparation of trimethylsilanyl-propiolic acid ethyl ester by reacting with carbonochloridic acid ethyl ester as well as in the synthesis of iodoalkenes by radical addition of perfluoroalkyl iodides. It is used as a nucleophile in Friedel-Crafts type acylat</p>Fórmula:C5H10SiPureza:98%Forma y color:Clear colorless, LiquidPeso molecular:98.22Trimethylsilylacetylene
CAS:<p>S18950 - Trimethylsilylacetylene</p>Fórmula:C5H10SiPureza:98%Forma y color:Liquid, Clear LiquidPeso molecular:98.22(Trimethylsilyl)acetylene
CAS:<p>(Trimethylsilyl)acetylene</p>Fórmula:C5H10SiPureza:97%Forma y color: clear. colourless liquidPeso molecular:98.2184g/molTrimethylsilylacetylene
CAS:<p>Trimethylsilylacetylene is a chemical compound that belongs to the class of organic compounds. It is an intermediate in the production of fatty acids and has been shown to be involved in the metabolism of other compounds, such as halides. Trimethylsilylacetylene is also used to inhibit inflammatory diseases and metabolic disorders, such as diabetes mellitus and Alzheimer's disease. Trimethylsilylacetylene inhibits replication by binding to the amine group on purine bases or DNA at the replication fork. This prevents DNA synthesis, which prevents cell division, causing cells to die. Trimethylsilylacetylene also inhibits cell division by reacting with carbonyl groups on proteins during replication.</p>Fórmula:C5H10SiPureza:Min. 95%Forma y color:Colorless Clear LiquidPeso molecular:98.22 g/molEthynyltrimethylsilane
CAS:Producto controlado<p>Applications Ethynyltrimethylsilane is used in the production of novel histone deacetylase inhibitors for the treatment of Freidreich’s ataxia. It also aids in the preparation of conjugated polymers with sn anthracene backbone.<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 Xu, C. et al.: Pharmaceu. 4, 1578 (2011); Kobayashi, E. et al.: J. Polym. Sci. Part A: Polym. Chem., 28, 2641 (1990);<br></p>Fórmula:C5H10SiForma y color:NeatPeso molecular:98.22






