(S)-1-(tert-butoxycarbonyl)-2,3-oxiranylmethylamine

98%

Reagent Code: #235875
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CAS Number 161513-47-9

science Other reagents with same CAS 161513-47-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.2096 g/mol
Formula C₈H₁₅NO₃
badge Registry Numbers
MDL Number MFCD06200796
thermostat Physical Properties
Melting Point 48 - 50 ℃
Boiling Point 262.9 ℃ at 760mmHg
inventory_2 Storage & Handling
Density 1.081 g/cm3
Storage 2-8°C

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in a stereocontrolled manner. The amine and Boc-protected groups facilitate peptide coupling and multistep synthesis, making it valuable in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Commonly employed in the preparation of HIV protease inhibitors and renin inhibitors for hypertension treatment.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,220.00
inventory 250mg
10-20 days ฿4,570.00
inventory 1g
10-20 days ฿12,870.00

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(S)-1-(tert-butoxycarbonyl)-2,3-oxiranylmethylamine
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Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in a stereocontrolled manner. The amine and Boc-protected groups facilitate peptide coupling and multistep synthesis, making it valuable in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Commonly employ

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in a stereocontrolled manner. The amine and Boc-protected groups facilitate peptide coupling and multistep synthesis, making it valuable in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Commonly employed in the preparation of HIV protease inhibitors and renin inhibitors for hypertension treatment.

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