(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid

≥95%

Reagent Code: #38378
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CAS Number 159990-12-2

science Other reagents with same CAS 159990-12-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₅H₂₁NO₅
badge Registry Numbers
MDL Number MFCD03427900
thermostat Physical Properties
Boiling Point 463.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxyphenyl moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. It is often employed in the preparation of compounds targeting neurological disorders, inflammation, and other therapeutic areas. Additionally, its chiral center enables the production of enantiomerically pure substances, which is critical for drug efficacy and safety.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,398.00
inventory 250mg
10-20 days ฿2,961.00
inventory 5g
10-20 days ฿22,770.00

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(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxyphenyl moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. It is often employed in the preparation of compounds targ

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxyphenyl moiety, makes it valuable in peptide synthesis and medicinal chemistry. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. It is often employed in the preparation of compounds targeting neurological disorders, inflammation, and other therapeutic areas. Additionally, its chiral center enables the production of enantiomerically pure substances, which is critical for drug efficacy and safety.

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