3-tert-Butyl 8-methyl 3-azabicyclo[3.2.1]octane-3,8-dicarboxylate

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Reagent Code: #150381
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CAS Number 1403766-87-9

science Other reagents with same CAS 1403766-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.34 g/mol
Formula C₁₄H₂₃NO₄
badge Registry Numbers
MDL Number MFCD23106312
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for conformational restriction, helping to enhance selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of bioactive molecules where the tert-butyl and methyl ester groups can be selectively deprotected or modified to introduce functional handles for further derivatization. Also utilized in asymmetric synthesis due to its chiral framework, supporting the creation of enantiomerically pure compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,810.00
inventory 250mg
10-20 days ฿5,390.00
inventory 1g
10-20 days ฿21,460.00

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3-tert-Butyl 8-methyl 3-azabicyclo[3.2.1]octane-3,8-dicarboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for conformational restriction, helping to enhance selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of bioactive molecules where the tert-butyl and methyl ester groups can be selectively deprotected or modified to introduce functional handles for further derivatization.
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for conformational restriction, helping to enhance selectivity and metabolic stability in drug candidates. Commonly employed in the preparation of bioactive molecules where the tert-butyl and methyl ester groups can be selectively deprotected or modified to introduce functional handles for further derivatization. Also utilized in asymmetric synthesis due to its chiral framework, supporting the creation of enantiomerically pure compounds.
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