(R)-tert-butyl 2-((benzyloxy)methyl)morpholine-4-carboxylate

95%

Reagent Code: #230900
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CAS Number 135097-68-6

science Other reagents with same CAS 135097-68-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.39 g/mol
Formula C₁₇H₂₅NO₄
badge Registry Numbers
MDL Number MFCD14635672
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules requiring stereochemical control. Its protected alcohol and amine functionalities make it valuable in peptide-like coupling reactions and in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in protease inhibitors and central nervous system agents. The benzyl and tert-butoxycarbonyl (Boc) protecting groups allow selective deprotection and further functionalization, enabling stepwise assembly of multi-step synthetic pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿17,890.00
250mg
10-20 days ฿31,800.00
1g
10-20 days ฿63,610.00
(R)-tert-butyl 2-((benzyloxy)methyl)morpholine-4-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules requiring stereochemical control. Its protected alcohol and amine functionalities make it valuable in peptide-like coupling reactions and in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in protease inhibitors and central nervous system agents. The benzyl and tert-butoxycarbonyl (Boc) prot

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules requiring stereochemical control. Its protected alcohol and amine functionalities make it valuable in peptide-like coupling reactions and in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in protease inhibitors and central nervous system agents. The benzyl and tert-butoxycarbonyl (Boc) protecting groups allow selective deprotection and further functionalization, enabling stepwise assembly of multi-step synthetic pathways.

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