6-Hydroxy-2-azaspiro[3.3]heptane-2-carboxylic acid tert-butyl ester

98%

Reagent Code: #75731
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CAS Number 1147557-97-8

science Other reagents with same CAS 1147557-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.28 g/mol
Formula C₁₁H₁₉NO₃
badge Registry Numbers
MDL Number MFCD15071431
thermostat Physical Properties
Melting Point 127-129℃
inventory_2 Storage & Handling
Density 1.17g/ml
Storage 2-8℃, sealed, dry

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its unique spirocyclic structure makes it valuable for designing and producing novel drug candidates, especially in the field of medicinal chemistry. Researchers often employ it to create compounds targeting neurological disorders, as its structural features can interact with specific biological receptors. Additionally, it serves as a building block in organic synthesis, enabling the creation of diverse chemical entities with potential therapeutic applications. Its tert-butyl ester group provides stability during synthetic processes, making it a practical choice for multi-step reactions.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 97.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿387.00
inventory 250mg
10-20 days ฿648.00
inventory 1g
10-20 days ฿2,007.00
inventory 5g
10-20 days ฿6,705.00

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6-Hydroxy-2-azaspiro[3.3]heptane-2-carboxylic acid tert-butyl ester
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This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its unique spirocyclic structure makes it valuable for designing and producing novel drug candidates, especially in the field of medicinal chemistry. Researchers often employ it to create compounds targeting neurological disorders, as its structural features can interact with specific biological receptors. Additionally, it serves as a building block in organic synthesis, enabling the creation of diverse chemical entities with potential therapeutic applications. Its tert-butyl ester group provides stability during synthetic processes, making it a practical choice for multi-step reactions.
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