3-tert-Butoxycarbonylamino-3-(3-chlorophenyl)propionic acid

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Reagent Code: #145781
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CAS Number 284493-67-0

science Other reagents with same CAS 284493-67-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.75 g/mol
Formula C₁₄H₁₈ClNO₄
badge Registry Numbers
MDL Number MFCD02090710
thermostat Physical Properties
Melting Point 95-96°C
Boiling Point 445.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective modification in peptide-based drug design, making it valuable in medicinal chemistry research. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc (tert-butoxycarbonyl) protecting group, which enables controlled deprotection and coupling steps. Also utilized in the preparation of enzyme inhibitors and receptor ligands targeting neurological and metabolic disorders.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿770.00
inventory 1g
10-20 days ฿2,150.00
inventory 5g
10-20 days ฿8,030.00

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3-tert-Butoxycarbonylamino-3-(3-chlorophenyl)propionic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective modification in peptide-based drug design, making it valuable in medicinal chemistry research. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc (tert-butoxycarbonyl) protecting group, which enables controlled deprotection and coupling steps. Also utilized

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective modification in peptide-based drug design, making it valuable in medicinal chemistry research. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc (tert-butoxycarbonyl) protecting group, which enables controlled deprotection and coupling steps. Also utilized in the preparation of enzyme inhibitors and receptor ligands targeting neurological and metabolic disorders.

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