(3R,4R)-1-Benzyl-4-Fluoropyrrolidin-3-Amine Bis(4-Methylbenzenesulfonate)

95%

Reagent Code: #231707
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CAS Number 1776113-98-4

science Other reagents with same CAS 1776113-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 538.65 g/mol
Formula C₂₅H₃₁FN₂O₆S₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and hydroxyl-like functionality make it suitable for peptide-like coupling reactions and heterocycle formation. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to its ability to mimic natural amino acid structures while enhancing metabolic stability. The bis(tosylate) groups allow for selective deprotection and further functionalization in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,700.00
(3R,4R)-1-Benzyl-4-Fluoropyrrolidin-3-Amine Bis(4-Methylbenzenesulfonate)
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and hydroxyl-like functionality make it suitable for peptide-like coupling reactions and heterocycle formation. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to its ability to mimic natural amino acid structures while enhancing metabolic stability. The bis

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and hydroxyl-like functionality make it suitable for peptide-like coupling reactions and heterocycle formation. Commonly employed in the preparation of protease inhibitors and central nervous system agents due to its ability to mimic natural amino acid structures while enhancing metabolic stability. The bis(tosylate) groups allow for selective deprotection and further functionalization in multi-step syntheses.

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