(S)-3-Phenyl-2-(undec-10-enamido)propanoic acid

97%

Reagent Code: #237640
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CAS Number 175357-18-3

science Other reagents with same CAS 175357-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.455 g/mol
Formula C₂₀H₂₉NO₃
thermostat Physical Properties
Melting Point 109-112 °C
Boiling Point 540.0±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.047±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of certain bioactive molecules, particularly in the development of peptidomimetic drugs. Its structure allows for selective interactions with enzyme active sites, making it valuable in designing inhibitors for proteases involved in disease pathways. The presence of the terminal alkene group enables further functionalization via click chemistry or cross-metathesis, facilitating conjugation to carriers or labeling with probes in medicinal chemistry research. It is also employed in the preparation of chiral building blocks for asymmetric synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,840.00
inventory 100g
10-20 days ฿6,480.00
(S)-3-Phenyl-2-(undec-10-enamido)propanoic acid
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Used as a key intermediate in the synthesis of certain bioactive molecules, particularly in the development of peptidomimetic drugs. Its structure allows for selective interactions with enzyme active sites, making it valuable in designing inhibitors for proteases involved in disease pathways. The presence of the terminal alkene group enables further functionalization via click chemistry or cross-metathesis, facilitating conjugation to carriers or labeling with probes in medicinal chemistry research. It i

Used as a key intermediate in the synthesis of certain bioactive molecules, particularly in the development of peptidomimetic drugs. Its structure allows for selective interactions with enzyme active sites, making it valuable in designing inhibitors for proteases involved in disease pathways. The presence of the terminal alkene group enables further functionalization via click chemistry or cross-metathesis, facilitating conjugation to carriers or labeling with probes in medicinal chemistry research. It is also employed in the preparation of chiral building blocks for asymmetric synthesis.

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