(R)-1-CBZ-5-OXO-PIPERIDINE-2-CARBOXYLIC ACID METHYL ESTER

98%

Reagent Code: #232340
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CAS Number 1638744-71-4

science Other reagents with same CAS 1638744-71-4

blur_circular Chemical Specifications

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Weight 291.30 g/mol
Formula C₁₅H₁₇NO₅
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MDL Number MFCD27987088
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine (CBZ) and ester functionalities allow for selective transformations in multi-step organic syntheses. Commonly employed in the preparation of neuroactive compounds and antiviral agents due to its structural compatibility with peptidomimetic frameworks. The compound’s stereochemistry enables high enantioselectivity in final drug candidates, making it valuable in medicinal chemistry for optimizing potency and reducing off-target effects.

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inventory 250mg
10-20 days ฿20,720.00

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(R)-1-CBZ-5-OXO-PIPERIDINE-2-CARBOXYLIC ACID METHYL ESTER
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine (CBZ) and ester functionalities allow for selective transformations in multi-step organic syntheses. Commonly employed in the preparation of neuroactive compounds and antiviral agents due to its structural compatibility with peptidomimetic frameworks. The compound’s stereochemistry enables high enantioselectivity in final drug can

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine (CBZ) and ester functionalities allow for selective transformations in multi-step organic syntheses. Commonly employed in the preparation of neuroactive compounds and antiviral agents due to its structural compatibility with peptidomimetic frameworks. The compound’s stereochemistry enables high enantioselectivity in final drug candidates, making it valuable in medicinal chemistry for optimizing potency and reducing off-target effects.

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