(S)-Benzyl 4-amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoate

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Reagent Code: #50212
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CAS Number 13512-57-7

science Other reagents with same CAS 13512-57-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.36 g/mol
Formula C₁₆H₂₂N₂O₅
badge Registry Numbers
MDL Number MFCD00190784
thermostat Physical Properties
Boiling Point 538.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used in the synthesis of peptides and pharmaceutical intermediates, particularly in the production of chiral compounds. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific amino acid structures. Commonly employed in medicinal chemistry for designing drugs with targeted biological activities, such as enzyme inhibitors or receptor modulators. Its protective groups, like the tert-butoxycarbonyl (Boc) group, enable selective reactions during complex organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿828.00
inventory 5g
10-20 days ฿9,405.00
inventory 250mg
10-20 days ฿1,242.00
inventory 1g
10-20 days ฿3,105.00

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(S)-Benzyl 4-amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoate
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Used in the synthesis of peptides and pharmaceutical intermediates, particularly in the production of chiral compounds. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific amino acid structures. Commonly employed in medicinal chemistry for designing drugs with targeted biological activities, such as enzyme inhibitors or receptor modulators. Its protective groups, like the tert-butoxycarbonyl (Boc) group, enable selective r
Used in the synthesis of peptides and pharmaceutical intermediates, particularly in the production of chiral compounds. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific amino acid structures. Commonly employed in medicinal chemistry for designing drugs with targeted biological activities, such as enzyme inhibitors or receptor modulators. Its protective groups, like the tert-butoxycarbonyl (Boc) group, enable selective reactions during complex organic syntheses.
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