(S)-4-NITROPHENYLALANINE METHYL ESTER HYDROCHLORIDE

98%

Reagent Code: #235800
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CAS Number 67877-95-6

science Other reagents with same CAS 67877-95-6

blur_circular Chemical Specifications

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Weight 260.67 g/mol
Formula C₁₀H₁₃ClN₂O₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in the synthesis of peptidomimetic drugs and bioactive molecules, particularly in the development of enzyme inhibitors and receptor ligands. Its chiral (S)-configuration makes it valuable in asymmetric synthesis for pharmaceuticals where stereochemistry affects biological activity. Commonly employed as an intermediate in the preparation of protease inhibitors and in solid-phase peptide synthesis due to the protected ester group and activated aromatic ring for further functionalization. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving amino acid derivatives.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿4,270.00
inventory 25g
10-20 days ฿14,520.00

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(S)-4-NITROPHENYLALANINE METHYL ESTER HYDROCHLORIDE
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Used in the synthesis of peptidomimetic drugs and bioactive molecules, particularly in the development of enzyme inhibitors and receptor ligands. Its chiral (S)-configuration makes it valuable in asymmetric synthesis for pharmaceuticals where stereochemistry affects biological activity. Commonly employed as an intermediate in the preparation of protease inhibitors and in solid-phase peptide synthesis due to the protected ester group and activated aromatic ring for further functionalization. Also utilized

Used in the synthesis of peptidomimetic drugs and bioactive molecules, particularly in the development of enzyme inhibitors and receptor ligands. Its chiral (S)-configuration makes it valuable in asymmetric synthesis for pharmaceuticals where stereochemistry affects biological activity. Commonly employed as an intermediate in the preparation of protease inhibitors and in solid-phase peptide synthesis due to the protected ester group and activated aromatic ring for further functionalization. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies involving amino acid derivatives.

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