추천 제품
Quality Level
분석
99%
형태
liquid
포함
Na2CO3 as stabilizer
refractive index
n20/D 1.444 (lit.)
bp
70-75 °C/2.5 mmHg (lit.)
density
1.115 g/mL at 25 °C (lit.)
작용기
bromo
저장 온도
2-8°C
SMILES string
CC(C)(C)[Si](C)(C)OCCBr
InChI
1S/C8H19BrOSi/c1-8(2,3)11(4,5)10-7-6-9/h6-7H2,1-5H3
InChI key
JBKINHFZTVLNEM-UHFFFAOYSA-N
일반 설명
(2-Bromoethoxy)-tert-butyldimethylsilane is a silane derivative.
애플리케이션
(2-Bromoethoxy)-tert-butyldimethylsilane was used in the synthesis of 4-(3-hydroxypropyl)-4′-methyl-2,2′-bipyridine.
It may be used as a reagent for the selective N-alkylation of 5-piperazin-1-yl-1H-indole and (1H-indol-2-yl)-piperazin-1-yl-methanone and also in the synthesis of 2-[3-[(3,4,5-trimethoxyphenyl)thio]-1H-indol-5-yloxy]ethanol.
It may be used as a reagent for the selective N-alkylation of 5-piperazin-1-yl-1H-indole and (1H-indol-2-yl)-piperazin-1-yl-methanone and also in the synthesis of 2-[3-[(3,4,5-trimethoxyphenyl)thio]-1H-indol-5-yloxy]ethanol.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
163.4 °F - closed cup
Flash Point (°C)
73 °C - closed cup
이미 열람한 고객
Journal of the American Chemical Society, 127(38), 13148-13149 (2005-09-22)
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 indoles were synthesized in good yields from
Tetrahedron Letters, 47(1), 69-72 (2005)
Arylthioindole inhibitors of tubulin polymerization. 3. Biological evaluation, structure-activity relationships and molecular modeling studies.
Journal of Medicinal Chemistry, 50(12), 2865-2874 (2007)
Tetrahedron Letters, 47, 69-69 (2006)
Journal of medicinal chemistry, 55(12), 5826-5840 (2012-05-31)
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 evaluate affinity (K(i)) of test compounds. Functional activity
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