N-Butoxycarbonyl trimethylphosphonoglycine

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Reagent Code: #217104
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CAS Number 89524-98-1

science Other reagents with same CAS 89524-98-1

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scatter_plot Molecular Information
Weight 297.24 g/mol
Formula C₁₀H₂₀NO₇P
badge Registry Numbers
MDL Number MFCD02178893
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key reagent in organic synthesis, particularly in the preparation of α,β-unsaturated amino acids through Horner-Wadsworth-Emmons olefination reactions. Its phosphonate group enables selective formation of olefins under mild conditions, making it valuable in peptide mimetic and pharmaceutical synthesis. The N-Boc protecting group ensures compatibility with multi-step synthetic sequences by preventing unwanted side reactions at the amino group. Commonly employed in the construction of complex molecules where stereocontrol and functional group tolerance are critical.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿510.00
inventory 25g
10-20 days ฿2,270.00
inventory 500g
10-20 days ฿44,400.00
inventory 100g
10-20 days ฿9,060.00

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N-Butoxycarbonyl trimethylphosphonoglycine
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Used as a key reagent in organic synthesis, particularly in the preparation of α,β-unsaturated amino acids through Horner-Wadsworth-Emmons olefination reactions. Its phosphonate group enables selective formation of olefins under mild conditions, making it valuable in peptide mimetic and pharmaceutical synthesis. The N-Boc protecting group ensures compatibility with multi-step synthetic sequences by preventing unwanted side reactions at the amino group. Commonly employed in the construction of complex mol

Used as a key reagent in organic synthesis, particularly in the preparation of α,β-unsaturated amino acids through Horner-Wadsworth-Emmons olefination reactions. Its phosphonate group enables selective formation of olefins under mild conditions, making it valuable in peptide mimetic and pharmaceutical synthesis. The N-Boc protecting group ensures compatibility with multi-step synthetic sequences by preventing unwanted side reactions at the amino group. Commonly employed in the construction of complex molecules where stereocontrol and functional group tolerance are critical.

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