(S)-N-BOC-TERT-LEUCINOL

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Reagent Code: #235881
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CAS Number 153645-26-2

science Other reagents with same CAS 153645-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.3052 g/mol
Formula C₁₁H₂₃NO₃
badge Registry Numbers
MDL Number MFCD01861301
thermostat Physical Properties
Melting Point 102-103 °C
Boiling Point 313.7 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.986 g/cm3
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its free alcohol and BOC-protected amine groups make it ideal for peptide synthesis and asymmetric synthesis where stereochemistry control is critical. Commonly employed in the development of protease inhibitors and other therapeutic agents requiring high enantiomeric purity. The BOC-protected amine allows for selective deprotection and coupling in multi-step reactions, enhancing its utility in medicinal chemistry and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,800.00
inventory 25g
10-20 days ฿8,010.00
inventory 100g
10-20 days ฿32,020.00

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(S)-N-BOC-TERT-LEUCINOL
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Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its free alcohol and BOC-protected amine groups make it ideal for peptide synthesis and asymmetric synthesis where stereochemistry control is critical. Commonly employed in the development of protease inhibitors and other therapeutic agents requiring high enantiomeric purity. The BOC-protected amine allows for selective deprotection and coupling in multi-step reactions, enhancing its utility in medicina

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its free alcohol and BOC-protected amine groups make it ideal for peptide synthesis and asymmetric synthesis where stereochemistry control is critical. Commonly employed in the development of protease inhibitors and other therapeutic agents requiring high enantiomeric purity. The BOC-protected amine allows for selective deprotection and coupling in multi-step reactions, enhancing its utility in medicinal chemistry and drug discovery.

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