2-Amino-2-cyclobutylacetic acid

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Reagent Code: #135612
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CAS Number 28024-69-3

science Other reagents with same CAS 28024-69-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.16 g/mol
Formula C₆H₁₁NO₂
badge Registry Numbers
MDL Number MFCD09264350
thermostat Physical Properties
Melting Point 157-161°C
Boiling Point 240°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of β-lactam antibiotics and other bioactive molecules. Its constrained cyclobutyl ring enhances metabolic stability and influences conformational rigidity, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also explored in the design of enzyme inhibitors and peptidomimetics due to its structural similarity to natural amino acids while offering improved resistance to degradation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,060.00
inventory 250mg
10-20 days ฿2,590.00
inventory 1g
10-20 days ฿5,970.00
inventory 5g
10-20 days ฿28,120.00

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2-Amino-2-cyclobutylacetic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of β-lactam antibiotics and other bioactive molecules. Its constrained cyclobutyl ring enhances metabolic stability and influences conformational rigidity, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also explored in the design of enzyme inhibitors and peptidomimetics due to its structural similarity to natural amino acids while offering improved resistance to degrada

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of β-lactam antibiotics and other bioactive molecules. Its constrained cyclobutyl ring enhances metabolic stability and influences conformational rigidity, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also explored in the design of enzyme inhibitors and peptidomimetics due to its structural similarity to natural amino acids while offering improved resistance to degradation.

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