1-BOC-D-PYROGLUTAMIC ACID ETHYL ESTER

98%

Reagent Code: #144684
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CAS Number 144978-35-8

science Other reagents with same CAS 144978-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.284 g/mol
Formula C₁₂H₁₉NO₅
badge Registry Numbers
MDL Number MFCD09261329
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 peptide-based drugs and heterocyclic compounds. Its protected functional groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemistry is critical. The BOC group provides stability during synthesis and can be easily removed under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide coupling strategies. Also utilized in the production of nootropics and cognitive enhancers due to its structural similarity to pyroglutamate derivatives involved in neurological pathways.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 5g
10-20 days ฿180.00
inventory 25g
10-20 days ฿1,100.00
inventory 100g
10-20 days ฿3,100.00
inventory 500g
10-20 days ฿15,200.00

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1-BOC-D-PYROGLUTAMIC ACID ETHYL ESTER
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs and heterocyclic compounds. Its protected functional groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemistry is critical. The BOC group provides stability during synthesis and can be easily removed under mild acidic conditions, making it ideal for solid-phase

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of peptide-based drugs and heterocyclic compounds. Its protected functional groups allow for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemistry is critical. The BOC group provides stability during synthesis and can be easily removed under mild acidic conditions, making it ideal for solid-phase and solution-phase peptide coupling strategies. Also utilized in the production of nootropics and cognitive enhancers due to its structural similarity to pyroglutamate derivatives involved in neurological pathways.

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