endo-3-Boc-3-azabicyclo[3.1.0]hexane-6-carboxylic acid

98%

Reagent Code: #148890
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CAS Number 1401464-07-0

science Other reagents with same CAS 1401464-07-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.25 g/mol
Formula C₁₁H₁₇NO₄
badge Registry Numbers
MDL Number MFCD12198805
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its rigid bicyclic structure and functional groups make it valuable for constructing potent and selective drug candidates, especially in central nervous system agents and enzyme inhibitors. The Boc-protected amine allows for controlled deprotection and further derivatization in multi-step syntheses, enabling efficient route design in medicinal chemistry.

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Test Parameter Specification
Appearance White solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,590.00
250mg
10-20 days ฿7,700.00

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endo-3-Boc-3-azabicyclo[3.1.0]hexane-6-carboxylic acid
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its rigid bicyclic structure and functional groups make it valuable for constructing potent and selective drug candidates, especially in central nervous system agents and enzyme inhibitors. The Boc-protected amine allows for controlled deprotection and further derivatization in multi-step syntheses, enabling efficient route design in medicinal chemistry.

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its rigid bicyclic structure and functional groups make it valuable for constructing potent and selective drug candidates, especially in central nervous system agents and enzyme inhibitors. The Boc-protected amine allows for controlled deprotection and further derivatization in multi-step syntheses, enabling efficient route design in medicinal chemistry.

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