683434
(Dimethylphenylsilyl)boronic acid pinacol ester
95%
Sinonimo/i:
2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, B-(dimethylphenylsilyl)pinacolborane
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About This Item
Formula empirica (notazione di Hill):
C14H23BO2Si
Numero CAS:
Peso molecolare:
262.23
Numero MDL:
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
95%
Stato
liquid
Indice di rifrazione
n20/D 1.4946
Densità
0.962 g/mL at 25 °C
Stringa SMILE
CC1(C)OB(OC1(C)C)[Si](C)(C)c2ccccc2
InChI
1S/C14H23BO2Si/c1-13(2)14(3,4)17-15(16-13)18(5,6)12-10-8-7-9-11-12/h7-11H,1-6H3
ARMSAQNLTKGMGM-UHFFFAOYSA-N
Categorie correlate
Applicazioni
(Dimethylphenylsilyl)boronic acid pinacol ester (Suginome′s reagent) can be used as a reagent:
- For the selective addition of dimethylphenylsilanyl group to cyclic and acyclic unsaturated ketones, esters, acrylonitriles using a copper catalyst.
- In the synthesis of (Z)-4-boryl-1-silyl-2-alkene derivatives by stereoselective addition of silicon-boron bond to acyclic 1,3-dienes in presence of Ni catalyst.
- In the preparation of silyl-substituted butenoate and β-silyl-substituted acrylate derivatives from allenes and propiolate derivatives via hydrosilylation reactions using a copper catalyst.
- In the palladium-catalyzed asymmetric silaboration of allenes and alkanes to offered corresponding β-borylallylsilanes and 2-boryl-1-silylalkanes respectively.
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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Stereoselective 1, 4-silaboration of 1, 3-dienes catalyzed by nickel complexes
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Organic Letters, 1(10), 1567-1569 (1999)
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Angewandte Chemie (International Edition in English), 36(22), 2516-2518 (1997)
Palladium-catalyzed asymmetric silaboration of allenes.
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Journal of the American Chemical Society, 128(42), 13682-13683 (2006)
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