346225
(2-Methylpropyl)boronic acid
≥95.0%
Sinonimo/i:
Isobutaneboronic acid
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About This Item
Formula condensata:
(CH3)2CHCH2B(OH)2
Numero CAS:
Peso molecolare:
101.94
Numero MDL:
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
≥95.0%
Forma fisica
solid
Punto di fusione
108-111 °C (lit.)
Stringa SMILE
CC(C)CB(O)O
InChI
1S/C4H11BO2/c1-4(2)3-5(6)7/h4,6-7H,3H2,1-2H3
ZAZPDOYUCVFPOI-UHFFFAOYSA-N
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Categorie correlate
Applicazioni
(2-Methylpropyl)boronic acid can be used as:
It can also be used as a reactant in:
- A reactant in the preparation of 4-isobutylisoquinoline from 4-bromoisoquinoline by Suzuki-Miyaura type couple reaction.
- A catalyst along with aluminum hydroxide, boric acid in the polymerization of styrene.
It can also be used as a reactant in:
- Copper catalyzed cross-coupling reactions.
- The synthesis of polyborylalkanes by Ir-catalyzed C-H borylation reaction.
- The preparation of heterosubstituted diazaboroles and borinines.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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For the first time, a general catalytic procedure for the cross-coupling of primary amides and alkylboronic acids is demonstrated. The key to the success of this reaction was the identification of a mild base (NaOSiMe3) and oxidant (di-tert-butyl peroxide) to
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A transition-metal-free reductive hydroxymethylation reaction has been developed, enabling the preparation of tetrahydroisoquinolines bearing C4-quaternary centers from the corresponding isoquinolines. Deuterium labelling studies and control experiments enable a potential mechanism to be elucidated which features a key Cannizzaro-type reduction followed
Solution-state 15N NMR and solid-state single-crystal XRD study of heterosubstituted diazaboroles and borinines prepared via an effective and simple microwave-assisted solvent-free synthesis
Slabber CA, et al.
Journal of Organometallic Chemistry, 723, 122-128 (2013)
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