3,7,9-Triazabicyclo[3.3.1]nonane-3-carboxylic acid, 1,1-dimethylethylester

97%

Reagent Code: #238284
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CAS Number 868407-41-4

science Other reagents with same CAS 868407-41-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.31 g/mol
Formula C₁₁H₂₁N₃O₂
badge Registry Numbers
MDL Number MFCD23106402
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a rigid, nitrogen-containing scaffold. Its bicyclic structure enhances stability and selectivity in drug design. The ester group allows for easy modification, making it valuable in medicinal chemistry for creating libraries of compounds in structure-activity relationship studies. Also employed in the preparation of catalysts and ligands for asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,200.00
inventory 500mg
10-20 days ฿51,210.00

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3,7,9-Triazabicyclo[3.3.1]nonane-3-carboxylic acid, 1,1-dimethylethylester
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a rigid, nitrogen-containing scaffold. Its bicyclic structure enhances stability and selectivity in drug design. The ester group allows for easy modification, making it valuable in medicinal chemistry for creating libraries of compounds in structure-activity relationship studies. Also employed in the preparation of catalysts and ligands for asymmetric synthesi

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a rigid, nitrogen-containing scaffold. Its bicyclic structure enhances stability and selectivity in drug design. The ester group allows for easy modification, making it valuable in medicinal chemistry for creating libraries of compounds in structure-activity relationship studies. Also employed in the preparation of catalysts and ligands for asymmetric synthesis.

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