(R)-1,3'-Bipyrrolidine

98%

Reagent Code: #230574
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CAS Number 900164-95-6

science Other reagents with same CAS 900164-95-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.23 g/mol
Formula C₈H₁₆N₂
badge Registry Numbers
MDL Number MFCD11519103
thermostat Physical Properties
Boiling Point 215.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its rigid, bidentate amine structure makes it suitable as a ligand in asymmetric catalysis, enabling the production of enantiomerically pure compounds. Commonly employed in the synthesis of protease inhibitors and other bioactive molecules due to its ability to enhance binding selectivity and metabolic stability. Also utilized in the design of organocatalysts for carbon-carbon bond-forming reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,870.00
inventory 1g
10-20 days ฿13,560.00
inventory 250mg
10-20 days ฿3,910.00

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(R)-1,3'-Bipyrrolidine
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Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its rigid, bidentate amine structure makes it suitable as a ligand in asymmetric catalysis, enabling the production of enantiomerically pure compounds. Commonly employed in the synthesis of protease inhibitors and other bioactive molecules due to its ability to enhance binding selectivity and metabolic

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its rigid, bidentate amine structure makes it suitable as a ligand in asymmetric catalysis, enabling the production of enantiomerically pure compounds. Commonly employed in the synthesis of protease inhibitors and other bioactive molecules due to its ability to enhance binding selectivity and metabolic stability. Also utilized in the design of organocatalysts for carbon-carbon bond-forming reactions.

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