Sigma Aldrich Allylboronic Acid Pinacol Ester

Catalog No.	Quantity
32-464-71G	1 g
32-464-710G	10 g

Catalog No. 32-464-71G Supplier Sigma Aldrich Supplier No. 3246471G

Description

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

Reagent used forPalladium-catalyzed Suzuki-Miyaura cross-coupling reactions and olefin metathesis Intermolecular radical additions Allylboration of aldehydes catalyzed by chiral spirobiindane diol (SPINOL) based phosphoric acids Cobalt-catalyzed regioselective hydrovinylation of dienes with alkenes Nucleic acid-templated energy transfer leading to a photorelease reaction Stereoselective indium-catalyzed Hosomi-Sakurai reactions Reagent used in Preparation ofCyclic sulfone hydroxyethylamines as BACE1 inhibitors for reduction of Amyloid +a-Peptides Transmetalation of carbene Ru iodide with Ag carboxylates to give C-H-activated Ru carbene complexes as catalysts for Z-selective olefin metathesis Allylboronation reagent for the preparation of allylic alcohols, and homoallylic amines.

Specifications

• CAS: 72824-04-5
• Density: 0.896 g/mL at 25°C
• Boiling Point: 50°C to 53°C (5 mmHg, lit.)
• Molecular Formula: C9H17BO2
• Refractive Index: n20/D 1.4268
• Linear Formula: ((CH3)4C2O2)BCH2CH=CH2
• MDL Number: MFCD00013347
• Quantity: 1 g
• Synonym: 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; 4,4,5,5-tetramethyl-2-(2-propen-1-yl)-1,3,2-dioxaborolane; 4,4,5,5-tetramethyl-2-(2-propenyl)-1,3,2-dioxaborolane; Allyl pinacol boronate; Pinacol allylboronate; Pinacolyl 2-propenylboronate
• Molecular Weight (g/mol): 168.04 g/mol