(S)-tert-Butyl 2-(((benzyloxy)carbonyl)amino)-3-hydroxypropanoate

95%

Reagent Code: #233553
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CAS Number 59859-77-7

science Other reagents with same CAS 59859-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₅H₂₁NO₅
badge Registry Numbers
MDL Number MFCD03428467
thermostat Physical Properties
Melting Point 87.5 °C
Boiling Point 458.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.174±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of β-hydroxy-α-amino acid derivatives which are key structural motifs in various bioactive molecules. This serine derivative features a protected amine (Cbz) and carboxylic acid (tert-butyl ester), with a free hydroxyl group on the β-position, enabling selective reactions in peptide chemistry and asymmetric synthesis. Frequently utilized in the development of protease inhibitors and other enzyme-targeted drugs. Its (S) stereochemistry enables control over the configuration of final products, making it valuable in medicinal chemistry for creating enantiomerically pure compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,130.00
inventory 5g
10-20 days ฿8,000.00
inventory 25g
10-20 days ฿34,180.00
(S)-tert-Butyl 2-(((benzyloxy)carbonyl)amino)-3-hydroxypropanoate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of β-hydroxy-α-amino acid derivatives which are key structural motifs in various bioactive molecules. This serine derivative features a protected amine (Cbz) and carboxylic acid (tert-butyl ester), with a free hydroxyl group on the β-position, enabling selective reactions in peptide chemistry and asymmetric synthesis. Frequently utilized in the development of protease inhibitors and other enzyme-targeted

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of β-hydroxy-α-amino acid derivatives which are key structural motifs in various bioactive molecules. This serine derivative features a protected amine (Cbz) and carboxylic acid (tert-butyl ester), with a free hydroxyl group on the β-position, enabling selective reactions in peptide chemistry and asymmetric synthesis. Frequently utilized in the development of protease inhibitors and other enzyme-targeted drugs. Its (S) stereochemistry enables control over the configuration of final products, making it valuable in medicinal chemistry for creating enantiomerically pure compounds.

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