N-Boc-(2S,3S)-(-)-2-Amino-3-methyl-1-pentanol

95%

Reagent Code: #216605
label
Alias N-Boc-L-isoleucol;N-tert-butoxycarbonyl-L-isoleucol,N-Boc-(2S,3S)-(-)-2-amino-3-methyl-1-pentanol
fingerprint
CAS Number 106946-74-1

science Other reagents with same CAS 106946-74-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.31 g/mol
Formula C₁₁H₂₃NO₃
badge Registry Numbers
MDL Number MFCD00235929
thermostat Physical Properties
Boiling Point 121-126 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.984±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and protected amine group make it valuable for constructing complex molecules with high enantioselectivity. Commonly employed in medicinal chemistry for peptidomimetics and as an intermediate in the preparation of enzyme inhibitors. The Boc-protected amine allows for controlled deprotection and coupling in multi-step organic syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,090.00
10g
10-20 days ฿2,150.00
25g
10-20 days ฿4,660.00
250g
10-20 days ฿32,160.00
N-Boc-(2S,3S)-(-)-2-Amino-3-methyl-1-pentanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and protected amine group make it valuable for constructing complex molecules with high enantioselectivity. Commonly employed in medicinal chemistry for peptidomimetics and as an intermediate in the preparation of enzyme inhibitors. The Boc-protected amine allows for controlled deprotection and coupling in multi-step organic syntheses.
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