Tert-Butyl Spiro[Indoline-3,4'-Piperidine]-1-Carboxylate Hydrochloride

≥98%

Reagent Code: #241092
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CAS Number 1243474-66-9

science Other reagents with same CAS 1243474-66-9

blur_circular Chemical Specifications

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Weight 324.85 g/mol
Formula C₁₇H₂₅ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) agents. Its spirocyclic structure and tert-butyl carboxylate group provide conformational rigidity and protecting functionality, enhancing selectivity, metabolic stability, and ease of synthetic modification in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate bioavailability and binding affinity. Also utilized in the preparation of protease inhibitors and receptor antagonists in research settings.

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inventory 1g
10-20 days ฿8,530.00

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Tert-Butyl Spiro[Indoline-3,4'-Piperidine]-1-Carboxylate Hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) agents. Its spirocyclic structure and tert-butyl carboxylate group provide conformational rigidity and protecting functionality, enhancing selectivity, metabolic stability, and ease of synthetic modification in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate bioavaila

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) agents. Its spirocyclic structure and tert-butyl carboxylate group provide conformational rigidity and protecting functionality, enhancing selectivity, metabolic stability, and ease of synthetic modification in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate bioavailability and binding affinity. Also utilized in the preparation of protease inhibitors and receptor antagonists in research settings.

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