2-(3-(tert-Butoxycarbonyl)-3-azaspiro-[5.5]undecan-9-yl)acetic acid

95%

Reagent Code: #75155
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CAS Number 952480-32-9

science Other reagents with same CAS 952480-32-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.42 g/mol
Formula C₁₇H₂₉NO₄
badge Registry Numbers
MDL Number MFCD12198559
thermostat Physical Properties
Boiling Point 452.7℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.12g/ml
Storage Room temperature, sealed, ventilated

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those targeting neurological and psychiatric disorders. Its structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing rigid frameworks and enabling selective reactions in multi-step synthetic pathways. Additionally, it is employed in peptide chemistry, where the Boc group is used to protect amine functionalities during the synthesis of peptide chains. Its versatility and stability make it a crucial component in the production of bioactive compounds and drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿206,630.00
inventory 250mg
10-20 days ฿83,780.00

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2-(3-(tert-Butoxycarbonyl)-3-azaspiro-[5.5]undecan-9-yl)acetic acid
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This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those targeting neurological and psychiatric disorders. Its structure, featuring a spirocyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing rigid frameworks and enabling selective reactions in multi-step synthetic pathways. Additionally, it is employed in peptide chemistry, where the Boc group is used to protect amine functionalities during the synthesis of peptide chains. Its versatility and stability make it a crucial component in the production of bioactive compounds and drug candidates.
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