O-Acetyl-N-[(1,1-dimethylethoxy)carbonyl]-L-threonine

97%

Reagent Code: #222427
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CAS Number 45214-52-6

science Other reagents with same CAS 45214-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.27 g/mol
Formula C₁₁H₁₉NO₆
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MDL Number MFCD00151895
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in peptide synthesis, particularly in the preparation of complex pharmaceutical compounds where selective protection of functional groups is required. The tert-butoxycarbonyl (Boc) group provides stability during synthesis and can be removed under mild acidic conditions, making it ideal for stepwise assembly of peptides. The acetyl protection on the hydroxyl group prevents unwanted side reactions during coupling steps. Commonly applied in the production of bioactive peptides and investigational drugs requiring precise stereochemical control.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,890.00
O-Acetyl-N-[(1,1-dimethylethoxy)carbonyl]-L-threonine
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Used as an intermediate in peptide synthesis, particularly in the preparation of complex pharmaceutical compounds where selective protection of functional groups is required. The tert-butoxycarbonyl (Boc) group provides stability during synthesis and can be removed under mild acidic conditions, making it ideal for stepwise assembly of peptides. The acetyl protection on the hydroxyl group prevents unwanted side reactions during coupling steps. Commonly applied in the production of bioactive peptides and i

Used as an intermediate in peptide synthesis, particularly in the preparation of complex pharmaceutical compounds where selective protection of functional groups is required. The tert-butoxycarbonyl (Boc) group provides stability during synthesis and can be removed under mild acidic conditions, making it ideal for stepwise assembly of peptides. The acetyl protection on the hydroxyl group prevents unwanted side reactions during coupling steps. Commonly applied in the production of bioactive peptides and investigational drugs requiring precise stereochemical control.

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