Methyl 2-(S)-[N-Carbobenzyloxy]amino-3-aminopropionate, Hydrochloride

95%

Reagent Code: #38429
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CAS Number 35761-27-4

science Other reagents with same CAS 35761-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.7300 g/mol
Formula C₁₂H₁₇ClN₂O₄
badge Registry Numbers
MDL Number MFCD03701202
thermostat Physical Properties
Boiling Point 423.692 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.212g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a protected intermediate in organic and medicinal chemistry. It is particularly valuable in the preparation of complex peptides, where selective protection and deprotection of functional groups are required. The carbobenzyloxy (Cbz) group protects the amine functionality, allowing for controlled reactions at other sites of the molecule. This chemical is often employed in the development of pharmaceuticals, including protease inhibitors and other bioactive peptides, where precise structural modifications are critical for activity. Its hydrochloride form enhances solubility, facilitating its use in various reaction conditions.

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inventory 250mg
10-20 days ฿1,314.00

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Methyl 2-(S)-[N-Carbobenzyloxy]amino-3-aminopropionate, Hydrochloride
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This compound is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a protected intermediate in organic and medicinal chemistry. It is particularly valuable in the preparation of complex peptides, where selective protection and deprotection of functional groups are required. The carbobenzyloxy (Cbz) group protects the amine functionality, allowing for controlled reactions at other sites of the molecule. This chemical is often employed in the development of pharmaceuticals, including protease inhibitors and other bioactive peptides, where precise structural modifications are critical for activity. Its hydrochloride form enhances solubility, facilitating its use in various reaction conditions.
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