CAS 73183-34-3
:Bis(pinacolato)diborano
Descripción:
Bis(pinacolato)diborano, comúnmente conocido como B2pin2, es un compuesto organoboro caracterizado por su estructura y reactividad únicas. Presenta dos átomos de boro cada uno unido a un grupo pinacolato, que se deriva del pinacol, un diol. Este compuesto es típicamente un líquido incoloro a amarillo pálido y es conocido por su estabilidad en condiciones ambientales, lo que lo convierte en un reactivo valioso en la síntesis orgánica, particularmente en la formación de compuestos que contienen boro. B2pin2 se utiliza a menudo en reacciones de acilo cruzado, como el acilo Suzuki-Miyaura, debido a su capacidad para servir como fuente de boro. Su reactividad se puede atribuir a la presencia de los átomos de boro, que pueden sufrir diversas transformaciones, incluida la oxidación y la coordinación con otros nucleófilos. Además, Bis(pinacolato)diborano es soluble en disolventes orgánicos comunes, lo que mejora su utilidad en entornos de laboratorio. Se deben observar precauciones de seguridad al manipular este compuesto, ya que puede ser inflamable y puede representar riesgos para la salud si se inhala o ingiere.
Fórmula:C12H24B2O4
InChI:InChI=1S/C12H24B2O4/c1-9(2)10(3,4)16-13(15-9)14-17-11(5,6)12(7,8)18-14/h1-8H3
Clave InChI:InChIKey=IPWKHHSGDUIRAH-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)B2OC(C)(C)C(C)(C)O2
Sinónimos:- 1,3,2-Dioxaborolane, bimol. deriv.
- 2,2′-Bi-1,3,2-dioxaborolane, 4,4,4′,4′,5,5,5′,5′-octamethyl-
- 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 4,4,4',4',5,5,5',5'-Octamethyl-2,2'-Bi-1,3,2-Dioxaborolane
- 4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bi(1,3,2-dioxaborolane)
- 4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bi-1,3,2-dioxaborolan
- 4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bi-1,3,2-dioxaborolane [B<sub>2</sub>(pin)<sub>2</sub>]
- 4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bis(1,3,2-dioxaborolane)
- 4,4,5,5,4′,4′,5′,5′-Octamethyl-2,2′-Bi(1,3,2-Dioxaborolane)
- 4,4,5,5,4′,4′,5′,5′-Octamethyl-2,2′-bis(1,3,2-dioxaborolane)
- 4,4,5,5,4′,4′,5′,5′-Octamethyl-[2,2′]bi[[1,3,2]dioxaborolanyl]
- 4,4,5,5-Tetramethyl-1,3,2-dioxaborane
- 4,4,5,5-Tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane
- 4,4,5,5-Tetramethyl-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolan
- 4,4,5,5-Tetramethyl-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane
- 4,4′,5,5′-Octamethyl-2,2′-bi-1,3,2-dioxaborolane
- B<sub>2</sub>Pin<sub>2</sub>
- Bis(2,2,3,3-Tetramethyl-2,3-Butanedionato)Diboron
- Bis(4,4,5,5-tetramethyl-[1,3]dioxolan-2-yl)borane
- Bis(pinacolate)diboron
- Bis(pinacolato) diborate
- Bis(pinacolato)diborane
- Bis(pinacolato)diborane(4)
- Bis(pinanolato)diboron
- Bis-pinacoldiboron
- Bispinacolatodiboronmin
- Diboron Pinacol Ester
- Dipinacoldiboron
- Octamethyl-2,2′-bi(1,3,2-dioxaborolane)
- Pinacol diborane
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Encontrado 11 productos.
Bis(pinacolato)diboron
CAS:Fórmula:C12H24B2O4Pureza:>99.0%(GC)Forma y color:White to Almost white powder to crystalPeso molecular:253.94Bis(pinacolato)diboron, 98+%
CAS:<p>Bis(pinacolato)diboron is a reagent used for the cis-vicinal diborylation of acetylenes and olefins with platinum catalysis. It acts as a substrate used in a new palladium-catalyzed cyclization of 1,6-enynes leading to homoallylic alkylboronates. It is used as a condensation agent in the preparation</p>Fórmula:C12H24B2O4Pureza:98+%Forma y color:White to pale cream, Lumps and/or powderPeso molecular:253.94Bis(pinacolato)diboron
CAS:Bis(pinacolato)diboronFórmula:C12H24B2O4Pureza:99%Forma y color: white crystalline solidPeso molecular:253.93855g/molBis(pinacolato)diboron
CAS:Fórmula:C12H24B2O4Pureza:≥ 99.0%Forma y color:White or off-white crystalline powder or crystalsPeso molecular:253.94Bis(pinacolato)diboron, 99%
CAS:<p>Bis(pinacolato)diboron, 99%</p>Fórmula:C12H24B2O4Pureza:99%Forma y color:white to off-white xtl.Peso molecular:253.94Bis(pinacolato)diboron
CAS:<p>Bis(pinacolato)diboron is a versatile reagent that is used in organic synthesis. It is a boron-containing compound that inhibits the reaction between amines and hydroxide solutions, forming an intermediate copper complex with a carbonyl group. The mechanism of this inhibition has been explored and found to be due to the presence of a hydroxyl group on the bis(pinacolato)diboron molecule. Bis(pinacolato)diboron reacts with an amine to form an adduct containing a boron-nitrogen double bond. This intermediate then reacts with hydroxide ions from the solution to form the final product, which contains both an amine and hydroxyl groups. The isolated yield of this reaction is typically low, but can be increased by using palladium as a catalyst.</p>Fórmula:C12H24B2O4Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:253.94 g/molBis(pinacolato)diboron
CAS:<p>Applications Bis(pinacolato)diboron is used as a condensation agent in the preparation poly(arylene)s. Bis(pinacolato)diboron is an organoboranate with potential use as matrix metallo-proteinase (MMP-2) inhibitor.<br>References Ali, H.A. et al.: Arch. Pharm., 337, 183 (2004); Izumi, A. et al.: Chem. Lett., 7, 728 (2000);<br></p>Fórmula:C12H24B2O4Forma y color:White To Off-WhitePeso molecular:253.94Bis(pinacolato)diboron
CAS:<p>Bis(pinacolato)diboron is a reagent and building block in organic chemistry. It is a high-quality, versatile building block that can be used as a reactant or intermediate. This compound is used to synthesize complex compounds and fine chemicals. Bis(pinacolato)diboron has been shown to be an effective catalyst for the polymerization of ethylene oxide and propylene oxide, which are important precursors for polyurethanes and polyesters. The high quality of this compound makes it an excellent starting material for the synthesis of other compounds with similar properties.</p>Fórmula:C12H24B2O4Pureza:Min. 99 Area-%Peso molecular:253.94 g/mol









