(R)-ethyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate hydrochloride

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Reagent Code: #104287
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CAS Number 264235-79-2

science Other reagents with same CAS 264235-79-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.75 g/mol
Formula C₁₃H₁₉ClN₂O₄
badge Registry Numbers
MDL Number MFCD22573660
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of peptides and peptidomimetics. Its structure, featuring both amino and carbamate-protecting groups, makes it a valuable intermediate for constructing complex peptide chains. It is often employed in the preparation of bioactive molecules, including enzyme inhibitors and receptor agonists/antagonists, due to its ability to introduce specific chiral centers into the target molecules. Additionally, it is used in the development of prodrugs, where its ester functionality can be hydrolyzed in vivo to release the active drug. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,020.00
inventory 250mg
10-20 days ฿12,960.00
inventory 1g
10-20 days ฿23,130.00

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(R)-ethyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate hydrochloride
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of peptides and peptidomimetics. Its structure, featuring both amino and carbamate-protecting groups, makes it a valuable intermediate for constructing complex peptide chains. It is often employed in the preparation of bioactive molecules, including enzyme inhibitors and receptor agonists/antagonists, due to its ability to introduce specific chiral centers into the target molecules.

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of peptides and peptidomimetics. Its structure, featuring both amino and carbamate-protecting groups, makes it a valuable intermediate for constructing complex peptide chains. It is often employed in the preparation of bioactive molecules, including enzyme inhibitors and receptor agonists/antagonists, due to its ability to introduce specific chiral centers into the target molecules. Additionally, it is used in the development of prodrugs, where its ester functionality can be hydrolyzed in vivo to release the active drug. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions.

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