(S)-2-Amino-N-((S)-1-amino-1-oxo-3-phenylpropan-2-yl)-4-methylpentanamide hydrochloride

95%

Reagent Code: #38308
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CAS Number 74214-38-3

science Other reagents with same CAS 74214-38-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.8230 g/mol
Formula C₁₅H₂₄ClN₃O₂
badge Registry Numbers
MDL Number MFCD00238030
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the field of peptide synthesis, where it serves as a building block for creating complex peptide structures. Its specific stereochemistry makes it valuable in the production of enantiomerically pure peptides, which are crucial in pharmaceutical research and drug development. The compound is often employed in the synthesis of bioactive peptides that target specific receptors or enzymes, aiding in the study of biochemical pathways and the development of therapeutic agents. Additionally, its hydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions commonly required in peptide synthesis.

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inventory 100mg
10-20 days ฿2,007.00

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(S)-2-Amino-N-((S)-1-amino-1-oxo-3-phenylpropan-2-yl)-4-methylpentanamide hydrochloride
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This compound is primarily utilized in the field of peptide synthesis, where it serves as a building block for creating complex peptide structures. Its specific stereochemistry makes it valuable in the production of enantiomerically pure peptides, which are crucial in pharmaceutical research and drug development. The compound is often employed in the synthesis of bioactive peptides that target specific receptors or enzymes, aiding in the study of biochemical pathways and the development of therapeutic ag

This compound is primarily utilized in the field of peptide synthesis, where it serves as a building block for creating complex peptide structures. Its specific stereochemistry makes it valuable in the production of enantiomerically pure peptides, which are crucial in pharmaceutical research and drug development. The compound is often employed in the synthesis of bioactive peptides that target specific receptors or enzymes, aiding in the study of biochemical pathways and the development of therapeutic agents. Additionally, its hydrochloride form enhances solubility, facilitating its use in aqueous reaction conditions commonly required in peptide synthesis.

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