(S)-2-amino-3-methylbutanamide

98%

Reagent Code: #232550
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CAS Number 4540-60-7

science Other reagents with same CAS 4540-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 116.16 g/mol
Formula C₅H₁₂N₂O
badge Registry Numbers
MDL Number MFCD08669832
thermostat Physical Properties
Boiling Point 241.0±23.0 °C
inventory_2 Storage & Handling
Density 0.998±0.06 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and antiviral drugs. Its chiral amine structure makes it valuable for constructing stereoselective molecules in medicinal chemistry. Also employed as a building block in peptide mimetics to enhance metabolic stability and bioavailability. Commonly utilized in research settings for designing enzyme inhibitors due to its structural similarity to natural amino acids.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,330.00
inventory 250mg
10-20 days ฿2,530.00
inventory 1g
10-20 days ฿7,350.00
inventory 5g
10-20 days ฿24,240.00
(S)-2-amino-3-methylbutanamide
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and antiviral drugs. Its chiral amine structure makes it valuable for constructing stereoselective molecules in medicinal chemistry. Also employed as a building block in peptide mimetics to enhance metabolic stability and bioavailability. Commonly utilized in research settings for designing enzyme inhibitors due to its structural similarity to natural amino acids.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and antiviral drugs. Its chiral amine structure makes it valuable for constructing stereoselective molecules in medicinal chemistry. Also employed as a building block in peptide mimetics to enhance metabolic stability and bioavailability. Commonly utilized in research settings for designing enzyme inhibitors due to its structural similarity to natural amino acids.

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