(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid
≥95%
- Product Code: 38378
CAS:
159990-12-2
Molecular Weight: | 295.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₅ |
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EC Number: | MDL Number: | MFCD03427900 | |
Melting Point: | Boiling Point: | 463.2°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, dry and sealed |
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.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $116.44 |
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1.000 | 10-20 days | $290.93 |
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5.000 | 10-20 days | $895.45 |
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(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid
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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