(R)-Methyl 3-((tert-butoxycarbonyl)amino)butanoate

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Reagent Code: #37753
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CAS Number 159877-47-1

science Other reagents with same CAS 159877-47-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
badge Registry Numbers
MDL Number MFCD03788463
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require chiral specificity. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps in the controlled assembly of amino acids without unwanted side reactions. Additionally, it serves as an intermediate in the development of β-amino acid derivatives, which are important in designing drugs with enhanced metabolic stability and bioavailability. Its application is also seen in the preparation of compounds for biological studies, aiding in the exploration of enzyme interactions and receptor binding activities.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿11,592.00
inventory 10g
10-20 days ฿19,341.00
inventory 1g
10-20 days ฿3,843.00
inventory 250mg
10-20 days ฿1,530.00

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(R)-Methyl 3-((tert-butoxycarbonyl)amino)butanoate
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This compound is primarily used in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require chiral specificity. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps in the controlled assembly of amino acids without unwanted side reactions. Additionally, it serves as an intermediate in the development of β-amino acid derivatives, which are important in designing drugs w

This compound is primarily used in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require chiral specificity. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps in the controlled assembly of amino acids without unwanted side reactions. Additionally, it serves as an intermediate in the development of β-amino acid derivatives, which are important in designing drugs with enhanced metabolic stability and bioavailability. Its application is also seen in the preparation of compounds for biological studies, aiding in the exploration of enzyme interactions and receptor binding activities.

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