4-Azaspiro[2.4]heptane hemioxalate

95%

Reagent Code: #75556
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CAS Number 95442-76-5

science Other reagents with same CAS 95442-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284 g/mol
Formula ₂C₆H₁₁NC₂H₂O₄
badge Registry Numbers
MDL Number MFCD27987995
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in organic synthesis, this compound serves as a versatile building block for the development of complex molecular structures. Its spirocyclic framework is particularly valuable in the creation of novel pharmaceuticals, where it can impart unique conformational properties to drug molecules, potentially enhancing their efficacy and selectivity. Additionally, it finds application in the study of chemical reactions involving strained ring systems, aiding in the exploration of new reaction mechanisms and pathways. The hemioxalate form also facilitates its use in crystallization studies, contributing to the understanding of molecular packing and crystal engineering.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿4,986.00
inventory 10mg
10-20 days ฿7,479.00

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4-Azaspiro[2.4]heptane hemioxalate
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Used primarily in organic synthesis, this compound serves as a versatile building block for the development of complex molecular structures. Its spirocyclic framework is particularly valuable in the creation of novel pharmaceuticals, where it can impart unique conformational properties to drug molecules, potentially enhancing their efficacy and selectivity. Additionally, it finds application in the study of chemical reactions involving strained ring systems, aiding in the exploration of new reaction mech

Used primarily in organic synthesis, this compound serves as a versatile building block for the development of complex molecular structures. Its spirocyclic framework is particularly valuable in the creation of novel pharmaceuticals, where it can impart unique conformational properties to drug molecules, potentially enhancing their efficacy and selectivity. Additionally, it finds application in the study of chemical reactions involving strained ring systems, aiding in the exploration of new reaction mechanisms and pathways. The hemioxalate form also facilitates its use in crystallization studies, contributing to the understanding of molecular packing and crystal engineering.

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