(S)-4-tert-Butyl 3-methyl morpholine-3,4-dicarboxylate

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Reagent Code: #235976
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CAS Number 215917-98-9

science Other reagents with same CAS 215917-98-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.27 g/mol
Formula C₁₁H₁₉NO₅
badge Registry Numbers
MDL Number MFCD09756519
thermostat Physical Properties
Boiling Point 313.2±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules requiring stereochemical control. Its protected morpholine structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in asymmetric synthesis routes where the (S)-configuration is essential for biological activity. The tert-butyl and methyl ester groups facilitate stepwise deprotection and coupling reactions, enabling its incorporation into larger drug-like molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,000.00
inventory 1g
10-20 days ฿3,800.00
inventory 5g
10-20 days ฿18,350.00
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(S)-4-tert-Butyl 3-methyl morpholine-3,4-dicarboxylate
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules requiring stereochemical control. Its protected morpholine structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in asymmetric synthesis routes where the (S)-configuration is essential for biological activity. The tert-butyl and methyl ester groups facilitate stepwise d
Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules requiring stereochemical control. Its protected morpholine structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in asymmetric synthesis routes where the (S)-configuration is essential for biological activity. The tert-butyl and methyl ester groups facilitate stepwise deprotection and coupling reactions, enabling its incorporation into larger drug-like molecules.
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