(2-Bromoethoxy)-Tert-Butyldimethylsilane

(2-Bromoethoxy)-Tert-Butyldimethylsilane Structure
(2-Bromoethoxy)-Tert-Butyldimethylsilane structure
Common Name (2-Bromoethoxy)-Tert-Butyldimethylsilane
CAS Number 86864-60-0 Molecular Weight 239.225
Density 1.107 Boiling Point 191 ºC
Molecular Formula C8H19BrOSi Melting Point N/A
MSDS Chinese USA Flash Point 69 ºC
Symbol GHS07
GHS07
Signal Word Warning

Structure-activity relationship study of N⁶-(2-(4-(1H-Indol-5-yl)piperazin-1-yl)ethyl)-N⁶-propyl-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine analogues: development of highly selective D3 dopamine receptor agonists along with a highly potent D2/D3 agonist and their pharmacological characterization.

J. Med. Chem. 55(12) , 5826-40, (2012)

In our effort to develop multifunctional drugs against Parkinson's disease, a structure-activity-relationship study was carried out based on our hybrid molecular template targeting D2/D3 receptors. Competitive binding with [(3)H]spiroperidol was used to evalu...

A route to annulated indoles via a palladium-catalyzed tandem alkylation/direct arylation reaction.

J. Am. Chem. Soc. 127(38) , 13148-13149, (2005)

A norbornene-mediated palladium-catalyzed tandem alkylation/C-H functionalization sequence is described, in which an alkyl-aryl bond and a heteroaryl-aryl bond are formed in one pot. A variety of highly substituted six- and seven-membered ring annulated indol...

Hansen, Joshua; et al.

Tetrahedron Lett. 47(1) , 69-72, (2005)

Tetrahedron Lett. 47 , 69, (2006)

Synthesis, complete characterization, and enantioselective electrokinetic separation of functionalized ruthenium complex enantiomers. Holder E, et al.
Holder E, et al.

Chirality 16(6) , 363-368, (2004)

Arylthioindole inhibitors of tubulin polymerization. 3. Biological evaluation, structure-activity relationships and molecular modeling studies. La Regina G, et al.

J. Med. Chem. 50(12) , 2865-2874, (2007)