(-)-Sparteine sulfate pentahydrate

98%(HPLC)

Reagent Code: #235228
fingerprint
CAS Number 6160-12-9

science Other reagents with same CAS 6160-12-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 422.53 g/mol
Formula C₁₅H₂₆N₂·H₂SO₄·₅H₂O
badge Registry Numbers
MDL Number MFCD00149333
thermostat Physical Properties
Melting Point 134-141°C
Boiling Point 340.9°C
inventory_2 Storage & Handling
Storage 2-8ºC

description Product Description

Used as a chiral base in asymmetric synthesis, particularly in deprotonation reactions where stereochemical control is critical. Commonly employed in lithiation reactions to generate chiral organolithium reagents. Also serves as a ligand in transition metal catalysis, enhancing enantioselectivity in various organic transformations. Applied in the resolution of racemic mixtures, especially in pharmaceutical synthesis where enantiopurity is essential. Its utility extends to research settings for studying reaction mechanisms involving chiral intermediates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 20mg
10-20 days ฿1,974.50
inventory 100mg
10-20 days ฿3,261.50
inventory 500mg
10-20 days ฿7,370.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(-)-Sparteine sulfate pentahydrate
No image available

Used as a chiral base in asymmetric synthesis, particularly in deprotonation reactions where stereochemical control is critical. Commonly employed in lithiation reactions to generate chiral organolithium reagents. Also serves as a ligand in transition metal catalysis, enhancing enantioselectivity in various organic transformations. Applied in the resolution of racemic mixtures, especially in pharmaceutical synthesis where enantiopurity is essential. Its utility extends to research settings for studying r

Used as a chiral base in asymmetric synthesis, particularly in deprotonation reactions where stereochemical control is critical. Commonly employed in lithiation reactions to generate chiral organolithium reagents. Also serves as a ligand in transition metal catalysis, enhancing enantioselectivity in various organic transformations. Applied in the resolution of racemic mixtures, especially in pharmaceutical synthesis where enantiopurity is essential. Its utility extends to research settings for studying reaction mechanisms involving chiral intermediates.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...