(R)-4-Isopropyloxazolidine-2,5-dione

95%

Reagent Code: #228946
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CAS Number 43089-05-0

science Other reagents with same CAS 43089-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.14 g/mol
Formula C₆H₉NO₃
badge Registry Numbers
MDL Number MFCD03411321
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

The (R)-4-Isopropyloxazolidine-2,5-dione is the N-carboxyanhydride (NCA) of (R)-valine, a chiral reagent used in ring-opening polymerization (ROP) to synthesize optically active polypeptides and poly(amino acids). It facilitates the formation of peptide bonds with high stereochemical fidelity, preserving the chirality of the alpha-carbon. This compound is essential in the preparation of biomimetic materials, protein mimics, and pharmaceutical intermediates where defined stereochemistry is required. Polymerization typically proceeds under mild conditions using initiators like amines or metal catalysts, yielding polymers with controlled molecular weights and narrow polydispersity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿5,080.00
5g
10-20 days ฿15,250.00
25g
10-20 days ฿53,360.00
(R)-4-Isopropyloxazolidine-2,5-dione
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The (R)-4-Isopropyloxazolidine-2,5-dione is the N-carboxyanhydride (NCA) of (R)-valine, a chiral reagent used in ring-opening polymerization (ROP) to synthesize optically active polypeptides and poly(amino acids). It facilitates the formation of peptide bonds with high stereochemical fidelity, preserving the chirality of the alpha-carbon. This compound is essential in the preparation of biomimetic materials, protein mimics, and pharmaceutical intermediates where defined stereochemistry is required. Polymeri
The (R)-4-Isopropyloxazolidine-2,5-dione is the N-carboxyanhydride (NCA) of (R)-valine, a chiral reagent used in ring-opening polymerization (ROP) to synthesize optically active polypeptides and poly(amino acids). It facilitates the formation of peptide bonds with high stereochemical fidelity, preserving the chirality of the alpha-carbon. This compound is essential in the preparation of biomimetic materials, protein mimics, and pharmaceutical intermediates where defined stereochemistry is required. Polymerization typically proceeds under mild conditions using initiators like amines or metal catalysts, yielding polymers with controlled molecular weights and narrow polydispersity.
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