(R,R)-2,2′-Bipyrrolidine L-tartrate trihydrate

99%

Reagent Code: #230660
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CAS Number 137037-21-9

science Other reagents with same CAS 137037-21-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.36 g/mol
Formula C₈H₁₆N₂ · C₄H₆O₆ · ₃H₂O
badge Registry Numbers
MDL Number MFCD11656040
thermostat Physical Properties
Melting Point 117-118 °C (dec.) (lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as conjugate additions and aldol reactions. Its rigid structure and well-defined stereochemistry make it effective in inducing high enantioselectivity when complexed with metals like copper or nickel. Commonly employed in pharmaceutical synthesis where precise stereochemical control is critical. The tartrate salt form enhances solubility and stability, facilitating handling and reproducibility in reaction conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,550.00
inventory 1g
10-20 days ฿17,950.00

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(R,R)-2,2′-Bipyrrolidine L-tartrate trihydrate
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as conjugate additions and aldol reactions. Its rigid structure and well-defined stereochemistry make it effective in inducing high enantioselectivity when complexed with metals like copper or nickel. Commonly employed in pharmaceutical synthesis where precise stereochemical control is critical. The tartrate salt form enhances solubility and stability, facilitating handling and reproducibility in reacti

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as conjugate additions and aldol reactions. Its rigid structure and well-defined stereochemistry make it effective in inducing high enantioselectivity when complexed with metals like copper or nickel. Commonly employed in pharmaceutical synthesis where precise stereochemical control is critical. The tartrate salt form enhances solubility and stability, facilitating handling and reproducibility in reaction conditions.

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