N-(Methoxycarbonyl)-D-Valine Methyl Ester

95%

Reagent Code: #220069
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CAS Number 153575-98-5

science Other reagents with same CAS 153575-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₈H₁₅NO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions without racemization. Its ester and carbamate functionalities stabilize the structure during solid-phase or solution-phase synthesis, making it valuable in producing pharmaceutical intermediates and bioactive peptides. Commonly employed in the development of enzyme inhibitors and metabolic analogs due to the steric bulk and chirality of the valine core. Also serves as a chiral building block in asymmetric synthesis for drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,150.00
inventory 250mg
10-20 days ฿24,050.00
N-(Methoxycarbonyl)-D-Valine Methyl Ester
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Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions without racemization. Its ester and carbamate functionalities stabilize the structure during solid-phase or solution-phase synthesis, making it valuable in producing pharmaceutical intermediates and bioactive peptides. Commonly employed in the development of enzyme inhibitors and metabolic analogs due to the steric bulk and chirality of the valine core. Also serves as a chiral building block in asymmetri

Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling reactions without racemization. Its ester and carbamate functionalities stabilize the structure during solid-phase or solution-phase synthesis, making it valuable in producing pharmaceutical intermediates and bioactive peptides. Commonly employed in the development of enzyme inhibitors and metabolic analogs due to the steric bulk and chirality of the valine core. Also serves as a chiral building block in asymmetric synthesis for drug discovery.

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