2-(tert-butoxycarbonyl)-2-azabicyclo[2.1.1]hexane-5-carboxylicacid

98%

Reagent Code: #244698
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CAS Number 1279894-35-7

science Other reagents with same CAS 1279894-35-7

blur_circular Chemical Specifications

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Weight 227.26 g/mol
Formula C₁₁H₁₇NO₄
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MDL Number MFCD19686565
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with constrained ring systems. Its bridged bicyclic structure imparts rigidity, making it valuable for modifying peptide-like structures to enhance metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for constructing protease inhibitors and central nervous system agents. The Boc-protected nitrogen allows for straightforward deprotection and further functionalization in multi-step syntheses. Its carboxylic acid group enables coupling reactions to form amides or esters, facilitating incorporation into larger molecular architectures.

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inventory 1g
10-20 days ฿25,110.00

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2-(tert-butoxycarbonyl)-2-azabicyclo[2.1.1]hexane-5-carboxylicacid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with constrained ring systems. Its bridged bicyclic structure imparts rigidity, making it valuable for modifying peptide-like structures to enhance metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for constructing protease inhibitors and central nervous system agents. The Boc-protected nitrogen allows for straightforward deprotection and fur

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with constrained ring systems. Its bridged bicyclic structure imparts rigidity, making it valuable for modifying peptide-like structures to enhance metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for constructing protease inhibitors and central nervous system agents. The Boc-protected nitrogen allows for straightforward deprotection and further functionalization in multi-step syntheses. Its carboxylic acid group enables coupling reactions to form amides or esters, facilitating incorporation into larger molecular architectures.

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