(-)-Ipc2B(allyl)borane solution

1 M in pentane

Reagent Code: #200388
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CAS Number 85116-38-7

science Other reagents with same CAS 85116-38-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.37 g/mol
Formula C₂₃H₃₉B
badge Registry Numbers
MDL Number MFCD09038448
thermostat Physical Properties
Boiling Point 35-36 °C
inventory_2 Storage & Handling
Density 0.638 g/mL at 25 °C
Storage 2-8°C

description Product Description

Widely used in asymmetric synthesis, this reagent enables highly enantioselective allylboration of aldehydes to produce homoallylic alcohols with excellent stereocontrol. It is particularly effective in the synthesis of chiral building blocks for pharmaceuticals and natural products. The reagent transfers an allyl group selectively to the aldehyde substrate, with the chiral ligand ensuring high enantiomeric excess. Its solution form allows for easy handling and precise dosing in reaction setups. Commonly applied in one-pot transformations and multistep sequences where stereochemistry is critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25ml
10-20 days ฿30,880.00
inventory 5ml
10-20 days ฿8,750.00
(-)-Ipc2B(allyl)borane solution
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Widely used in asymmetric synthesis, this reagent enables highly enantioselective allylboration of aldehydes to produce homoallylic alcohols with excellent stereocontrol. It is particularly effective in the synthesis of chiral building blocks for pharmaceuticals and natural products. The reagent transfers an allyl group selectively to the aldehyde substrate, with the chiral ligand ensuring high enantiomeric excess. Its solution form allows for easy handling and precise dosing in reaction setups. Commonly

Widely used in asymmetric synthesis, this reagent enables highly enantioselective allylboration of aldehydes to produce homoallylic alcohols with excellent stereocontrol. It is particularly effective in the synthesis of chiral building blocks for pharmaceuticals and natural products. The reagent transfers an allyl group selectively to the aldehyde substrate, with the chiral ligand ensuring high enantiomeric excess. Its solution form allows for easy handling and precise dosing in reaction setups. Commonly applied in one-pot transformations and multistep sequences where stereochemistry is critical.

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