Methyl (2R,3S)-3-(tert-butoxycarbonylamino)-2-hydroxy-3-phenylpropionate

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Reagent Code: #205874
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CAS Number 124605-42-1

science Other reagents with same CAS 124605-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₅H₂₁NO₅
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MDL Number MFCD09037385
inventory_2 Storage & Handling
Storage 2~8℃, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of protease inhibitors such as those used in antiviral therapies. Its Boc-protected amino group and methyl ester functionality allow for selective reactions in multi-step organic syntheses, while the free hydroxyl group enables further functionalization. Commonly employed in the development of HIV and hepatitis C treatments due to its ability to mimic amino acid structures in enzyme active sites. Also utilized in the preparation of peptidomimetic compounds for research in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,980.00
inventory 25g
10-20 days ฿9,390.00
inventory 100g
10-20 days ฿37,510.00

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Methyl (2R,3S)-3-(tert-butoxycarbonylamino)-2-hydroxy-3-phenylpropionate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of protease inhibitors such as those used in antiviral therapies. Its Boc-protected amino group and methyl ester functionality allow for selective reactions in multi-step organic syntheses, while the free hydroxyl group enables further functionalization. Commonly employed in the development of HIV and hepatitis C treatments due to its ability to mimic amino acid structures in enzyme active sites. Also uti

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of protease inhibitors such as those used in antiviral therapies. Its Boc-protected amino group and methyl ester functionality allow for selective reactions in multi-step organic syntheses, while the free hydroxyl group enables further functionalization. Commonly employed in the development of HIV and hepatitis C treatments due to its ability to mimic amino acid structures in enzyme active sites. Also utilized in the preparation of peptidomimetic compounds for research in medicinal chemistry.

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