Pinacolborane

Pinacolborane
  • CAS No.:25015-63-8
Other grades of this product :
Pinacolborane Basic information
Product Name:Pinacolborane
Synonyms:Pinacolatoborane;TetraMethyl-1,3,2-dioxab;Pinacolborane, 97%, stabilized;4,4,5,5-TetraMethyl-1,3,2-dioxaborolane 97%;4,4,5,5-TetraMethyl-1,3,2-dioxaborolane solution 1.0 M in THF;Pinacolborane (4,4,5,5-Tetramethyl-1,3,2-dioxaborolane);4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE;PINACOLBORANE
CAS:25015-63-8
MF:C6H13BO2
MW:127.98
EINECS:607-485-3
Product Categories:Boron Derivatives;Heterocycles
Mol File:25015-63-8.mol
Pinacolborane Chemical Properties
Boiling point 42-43 °C50 mm Hg(lit.)
density 0.882 g/mL at 25 °C(lit.)
vapor pressure 29-119.9hPa at 20-50℃
refractive index n20/D 1.396(lit.)
Fp 41 °F
storage temp. 2-8°C
solubility Miscible with ether, dichloromethane, tetrahydrofuran and organic solvents.
form Liquid
Specific Gravity0.882
color Clear colorless to light yellow
Sensitive Air Sensitive
BRN 7802871
Stability:Air Sensitive, Hygroscopic, Moisture Sensitive
CAS DataBase Reference25015-63-8(CAS DataBase Reference)
Safety Information
Hazard Codes F,Xi,Xn
Risk Statements 11-15-36/37/38-36/37-19-40
Safety Statements 16-43-8-37/39-26-33-29-36/37
RIDADR UN 3398 4.3/PG 2
WGK Germany 3
Hazard Note Highly Flammable/Keep Cold/Air Sensitive
HazardClass 4.3
PackingGroup II
HS Code 29209090
MSDS Information
ProviderLanguage
Pinacolborane English
SigmaAldrich English
ACROS English
ALFA English
Pinacolborane Usage And Synthesis
Chemical PropertiesClear colorless liquid
UsesPinacolborane is used for synthesis of unsymmetrical biaryls via aromatic C-H borylation-cross-coupling sequence.
UsesPinacolborane is used as a precursor of boronic esters by hydroboration or coupling reactions. It acts as a monofunctional hydroborating agent. It is used in the synthesis of unsymmetrical biaryls through aromatic C-H borylation-cross-coupling sequence. It is involved in the preparation of 4,4,5,5-tetramethyl-2-thiophen-2-yl-[1,3,2]dioxaborolane by reacting with 2-iodo-thiophene. Further, it is used to prepare vinylboronates by palladium-catalyzed coupling with alkenyl triflates and iodides.

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