(R)-Di-tert-butyl 2-(hydroxymethyl)piperazine-1,4-dicarboxylate

98%

Reagent Code: #230971
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CAS Number 1159598-21-6

science Other reagents with same CAS 1159598-21-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.39 g/mol
Formula C₁₅H₂₈N₂O₅
badge Registry Numbers
MDL Number MFCD28968067
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected piperazine structure with a hydroxymethyl group allows for selective functionalization, making it valuable in medicinal chemistry for creating enantiomerically pure compounds. Commonly employed in the preparation of drug candidates targeting viral infections and central nervous system disorders. The tert-butyl carbamate (Boc) groups provide stability during synthesis and can be selectively removed under mild acidic conditions, enabling stepwise construction of complex molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,170.00
inventory 250mg
10-20 days ฿10,490.00
inventory 1g
10-20 days ฿21,250.00
(R)-Di-tert-butyl 2-(hydroxymethyl)piperazine-1,4-dicarboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected piperazine structure with a hydroxymethyl group allows for selective functionalization, making it valuable in medicinal chemistry for creating enantiomerically pure compounds. Commonly employed in the preparation of drug candidates targeting viral infections and central nervous system disorders. The tert-butyl carbamate (Boc) groups provi

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected piperazine structure with a hydroxymethyl group allows for selective functionalization, making it valuable in medicinal chemistry for creating enantiomerically pure compounds. Commonly employed in the preparation of drug candidates targeting viral infections and central nervous system disorders. The tert-butyl carbamate (Boc) groups provide stability during synthesis and can be selectively removed under mild acidic conditions, enabling stepwise construction of complex molecules.

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