(R)-N-Acetyl-2-naphthylalanine

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Reagent Code: #230250
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CAS Number 37440-01-0

science Other reagents with same CAS 37440-01-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.28 g/mol
Formula C₁₅H₁₅NO₃
badge Registry Numbers
MDL Number MFCD00079678
thermostat Physical Properties
Boiling Point 530.7°C
inventory_2 Storage & Handling
Density 1.241g/mL
Storage  2-8°C

description Product Description

Used in the synthesis of chiral pharmaceuticals, particularly as a building block for protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in drug development. Commonly employed in research settings for designing enzyme inhibitors due to the naphthyl group’s strong binding affinity with hydrophobic pockets in proteins. Also utilized in the preparation of intermediates for antitumor agents and antiviral compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,020.00
inventory 5g
10-20 days ฿3,920.00
inventory 25g
10-20 days ฿13,980.00

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(R)-N-Acetyl-2-naphthylalanine
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Used in the synthesis of chiral pharmaceuticals, particularly as a building block for protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in drug development. Commonly employed in research settings for designing enzyme inhibitors due to the naphthyl group’s strong binding affinity with hydrophobic pockets in proteins. Also utilized in the preparation of intermediates for antitumor ag

Used in the synthesis of chiral pharmaceuticals, particularly as a building block for protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in drug development. Commonly employed in research settings for designing enzyme inhibitors due to the naphthyl group’s strong binding affinity with hydrophobic pockets in proteins. Also utilized in the preparation of intermediates for antitumor agents and antiviral compounds.

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