655090
3-Methyl-1-butylboronic acid
Synonyme(s) :
Isopentylboronic acid
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About This Item
Formule empirique (notation de Hill) :
C5H13BO2
Numéro CAS:
Poids moléculaire :
115.97
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :
Produits recommandés
Forme
solid
Pf
80-91 °C
Température de stockage
2-8°C
Chaîne SMILES
CC(C)CCB(O)O
InChI
1S/C5H13BO2/c1-5(2)3-4-6(7)8/h5,7-8H,3-4H2,1-2H3
Clé InChI
UVMWVBMFEDQYRW-UHFFFAOYSA-N
Application
Reactant for:
- Selective copper-promoted cross-coupling with aromatic amines
- Synthesis of indazole based analog sensitive Akt inhibitors
- Preparation of alkylarenes via tetraphosphine-palladium-catalyzed Suzuki cross-coupling with aryl halides
Autres remarques
Contains varying amounts of anhydride
Code de la classe de stockage
13 - Non Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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The etiological underpinnings of many CNS disorders are not well understood. This is likely due to the fact that individual diseases aggregate numerous pathological subtypes, each associated with a complex landscape of genetic risk factors. To overcome these challenges, researchers
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