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Bis(pinacolato)diboron, 98+%, Thermo Scientific Chemicals

Catalog Number AAL1608803
Click to view available options
Quantity:
1 g
5 g
25 g
73183-34-3
C12H24B2O4
253.94
MFCD00799570
IPWKHHSGDUIRAH-UHFFFAOYSA-N
bis pinacolato diboron, bis pinacolato diborane, 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi 1,3,2-dioxaborolane, pinacol diborane, diboron pinacol ester, b2pin2, 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1,3,2-dioxaborolane, 4,4,5,5-tetramethyl-2-tetramethyl-1,3,2-dioxaborolan-2-yl-1,3,2-dioxaborolane, bispinacolate diboron, unii-i906w26p4u
2733548
4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane
CC1(C)OB(OC1(C)C)B1OC(C)(C)C(C)(C)O1
73183-34-3
C12H24B2O4
253.94
MFCD00799570
IPWKHHSGDUIRAH-UHFFFAOYSA-N
bis pinacolato diboron, bis pinacolato diborane, 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi 1,3,2-dioxaborolane, pinacol diborane, diboron pinacol ester, b2pin2, 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1,3,2-dioxaborolane, 4,4,5,5-tetramethyl-2-tetramethyl-1,3,2-dioxaborolan-2-yl-1,3,2-dioxaborolane, bispinacolate diboron, unii-i906w26p4u
2733548
4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane
CC1(C)OB(OC1(C)C)B1OC(C)(C)C(C)(C)O1

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 of poly(arylene)s. It plays an essential role in Suzuki reaction and used as matrix metallo-proteinase (MMP-2) inhibitor.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
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 of poly(arylene)s. It plays an essential role in Suzuki reaction and used as matrix metallo-proteinase (MMP-2) inhibitor.

Solubility
Soluble in tetrahydrofuran, dichloromethane, toluene, hexane and heptane. Insoluble in water.

Notes
Incompatible with strong oxidizing agents.
TRUSTED_SUSTAINABILITY
Melting Point 133°C to 139°C
Quantity 1 g
Beilstein 7703552
Solubility Information Soluble in tetrahydrofuran,dichloromethane,toluene,hexane and heptane. Insoluble in water.
Formula Weight 253.94
Percent Purity ≥98%
Chemical Name or Material Bis(pinacolato)diboron
Hazard Category Warning
Hazard Statement GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Precautionary Statement GHS P Statement
P261-P280-P305+P351+P338-P304+P340-P405-P501a
Avoid breathing dust/fume/gas/mist/vapors/spray.
Wear protective gloves/protective clothing/eye protection/face protection.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing.
Store locked up.
Dispose of contents/container in accordance with local/regional/national/international regulations.
TSCA No
Recommended Storage Keep cold

RUO – Research Use Only

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