(R)-tert-Butyl 4,5-diamino-5-oxopentanoate

95%

Reagent Code: #229197
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CAS Number 70701-78-9

science Other reagents with same CAS 70701-78-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.25 g/mol
Formula C₉H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD29923737
thermostat Physical Properties
Boiling Point 357.1±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.090±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its amine and ester functionalities allow for selective derivatization, making it valuable in peptidomimetic research and the preparation of enzyme inhibitors. The (R)-configuration enables stereocontrolled reactions, which is critical in drug design where enantiopurity affects efficacy and safety. Commonly employed in multi-step organic syntheses to introduce functionalized amino acid motifs into larger molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿5,410.00
5g
10-20 days ฿50,840.00
1g
10-20 days ฿14,540.00
(R)-tert-Butyl 4,5-diamino-5-oxopentanoate
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Used as a chiral building block in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its amine and ester functionalities allow for selective derivatization, making it valuable in peptidomimetic research and the preparation of enzyme inhibitors. The (R)-configuration enables stereocontrolled reactions, which is critical in drug design where enantiopurity affects efficacy and safety. Commonly employed in multi-step organic syntheses to introduce functionali

Used as a chiral building block in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its amine and ester functionalities allow for selective derivatization, making it valuable in peptidomimetic research and the preparation of enzyme inhibitors. The (R)-configuration enables stereocontrolled reactions, which is critical in drug design where enantiopurity affects efficacy and safety. Commonly employed in multi-step organic syntheses to introduce functionalized amino acid motifs into larger molecules.

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