N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydride

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Reagent Code: #216953
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CAS Number 84793-24-8

science Other reagents with same CAS 84793-24-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.33 g/mol
Formula C₁₆H₁₉NO₅
badge Registry Numbers
MDL Number MFCD00272296
thermostat Physical Properties
Melting Point 69-73 °C
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in the synthesis of peptide-based pharmaceuticals, this compound enables the controlled addition of amino acid residues in solid-phase or solution-phase peptide coupling. Its activated carboxyanhydride group facilitates efficient amide bond formation without requiring additional coupling agents, making it valuable in the preparation of complex peptides with high purity. It is particularly useful in the development of angiotensin-converting enzyme (ACE) inhibitors and other bioactive peptides where precise stereochemistry and functional group compatibility are critical.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25g
10-20 days ฿1,590.00
100g
10-20 days ฿5,590.00
N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydride
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Used primarily as an intermediate in the synthesis of peptide-based pharmaceuticals, this compound enables the controlled addition of amino acid residues in solid-phase or solution-phase peptide coupling. Its activated carboxyanhydride group facilitates efficient amide bond formation without requiring additional coupling agents, making it valuable in the preparation of complex peptides with high purity. It is particularly useful in the development of angiotensin-converting enzyme (ACE) inhibitors and oth

Used primarily as an intermediate in the synthesis of peptide-based pharmaceuticals, this compound enables the controlled addition of amino acid residues in solid-phase or solution-phase peptide coupling. Its activated carboxyanhydride group facilitates efficient amide bond formation without requiring additional coupling agents, making it valuable in the preparation of complex peptides with high purity. It is particularly useful in the development of angiotensin-converting enzyme (ACE) inhibitors and other bioactive peptides where precise stereochemistry and functional group compatibility are critical.

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