(R)-Tert-Butyl 3-Methyl-1-Oxo-2,8-Diazaspiro[4.5]Decane-8-Carboxylate

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Reagent Code: #231564
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CAS Number 1548290-30-7

science Other reagents with same CAS 1548290-30-7

blur_circular Chemical Specifications

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Weight 268.35 g/mol
Formula C₁₄H₂₄N₂O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with central nervous system activity. Its spirocyclic structure and chiral center make it valuable in medicinal chemistry for designing potent and selective drug candidates. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl carbamate (Boc) group allows for easy protection of amines during peptide-like synthesis, enabling stepwise construction of complex molecules. Its stability under various reaction conditions supports use in multi-step organic syntheses.

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inventory 100mg
10-20 days ฿27,610.00

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(R)-Tert-Butyl 3-Methyl-1-Oxo-2,8-Diazaspiro[4.5]Decane-8-Carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with central nervous system activity. Its spirocyclic structure and chiral center make it valuable in medicinal chemistry for designing potent and selective drug candidates. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl carbamate (Boc) group allows for easy protection of ami

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with central nervous system activity. Its spirocyclic structure and chiral center make it valuable in medicinal chemistry for designing potent and selective drug candidates. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl carbamate (Boc) group allows for easy protection of amines during peptide-like synthesis, enabling stepwise construction of complex molecules. Its stability under various reaction conditions supports use in multi-step organic syntheses.

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