(3S,6R)-1-((Benzyloxy)Carbonyl)-6-Methylpiperidine-3-Carboxylic Acid

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Reagent Code: #237288
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CAS Number 1227916-29-1

science Other reagents with same CAS 1227916-29-1

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Weight 277.32 g/mol
Formula C₁₅H₁₉NO₄
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Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry makes it valuable for constructing complex drug structures with high enantioselectivity. Commonly employed in medicinal chemistry for peptidomimetic design, where it helps improve metabolic stability and binding affinity. Also utilized in the preparation of enzyme inhibitors targeting diseases such as hepatitis C and HIV. The presence of functional groups allows for further derivatization, making it a versatile intermediate in asymmetric synthesis and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,680.00
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(3S,6R)-1-((Benzyloxy)Carbonyl)-6-Methylpiperidine-3-Carboxylic Acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry makes it valuable for constructing complex drug structures with high enantioselectivity. Commonly employed in medicinal chemistry for peptidomimetic design, where it helps improve metabolic stability and binding affinity. Also utilized in the preparation of enzyme inhibitors targeting diseases such as hepatitis C and HIV.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry makes it valuable for constructing complex drug structures with high enantioselectivity. Commonly employed in medicinal chemistry for peptidomimetic design, where it helps improve metabolic stability and binding affinity. Also utilized in the preparation of enzyme inhibitors targeting diseases such as hepatitis C and HIV. The presence of functional groups allows for further derivatization, making it a versatile intermediate in asymmetric synthesis and drug discovery.

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