![]() (2-Bromoethoxy)-Tert-Butyldimethylsilane structure
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Common Name | (2-Bromoethoxy)-Tert-Butyldimethylsilane | ||
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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 |
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... |
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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... |
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Hansen, Joshua; et al.
Tetrahedron Lett. 47(1) , 69-72, (2005)
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Tetrahedron Lett. 47 , 69, (2006)
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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)
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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)
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