1'-(tert-Butoxycarbonyl)-4-oxospiro[chroman-2,4'-piperidine]-7-carboxylic acid

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Reagent Code: #38708
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CAS Number 1086398-20-0

science Other reagents with same CAS 1086398-20-0

blur_circular Chemical Specifications

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Weight 361.3900 g/mol
Formula C₁₉H₂₃NO₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the development of various therapeutic agents. Its unique structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in the synthesis of complex molecules, particularly those targeting neurological and cardiovascular diseases. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molecule. Additionally, the carboxylic acid moiety provides a handle for conjugation or modification, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Its application extends to the design of protease inhibitors and other bioactive compounds, where the spirocyclic framework can mimic natural substrates or stabilize specific conformations.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,317.00

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1'-(tert-Butoxycarbonyl)-4-oxospiro[chroman-2,4'-piperidine]-7-carboxylic acid
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This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the development of various therapeutic agents. Its unique structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in the synthesis of complex molecules, particularly those targeting neurological and cardiovascular diseases. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molec

This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the development of various therapeutic agents. Its unique structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in the synthesis of complex molecules, particularly those targeting neurological and cardiovascular diseases. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the molecule. Additionally, the carboxylic acid moiety provides a handle for conjugation or modification, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Its application extends to the design of protease inhibitors and other bioactive compounds, where the spirocyclic framework can mimic natural substrates or stabilize specific conformations.

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