N-Boc-L-cyclohexylglycinol

98%

Reagent Code: #217069
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CAS Number 107202-39-1

science Other reagents with same CAS 107202-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.34 g/mol
Formula C₁₃H₂₅NO₃
badge Registry Numbers
MDL Number MFCD04112591
thermostat Physical Properties
Melting Point 83-87°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

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 N-Boc protected amine and free primary alcohol groups allow selective deprotection of the amine and coupling reactions at the alcohol, making it valuable in peptide mimetics and medicinal chemistry. The cyclohexyl group provides steric bulk and lipophilicity, enhancing binding selectivity in drug design. Commonly employed in solid-phase and solution-phase synthesis of complex organic molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿590.00
5g
10-20 days ฿2,010.00
25g
10-20 days ฿8,820.00
N-Boc-L-cyclohexylglycinol
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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 N-Boc protected amine and free primary alcohol groups allow selective deprotection of the amine and coupling reactions at the alcohol, making it valuable in peptide mimetics and medicinal chemistry. The cyclohexyl group provides steric bulk and lipophilicity, enhancing binding selectivity in drug design. Commonly employed in solid-phase and solutio

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its N-Boc protected amine and free primary alcohol groups allow selective deprotection of the amine and coupling reactions at the alcohol, making it valuable in peptide mimetics and medicinal chemistry. The cyclohexyl group provides steric bulk and lipophilicity, enhancing binding selectivity in drug design. Commonly employed in solid-phase and solution-phase synthesis of complex organic molecules.

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