(R)-2-Aminopent-4-ynoic acid

98%

Reagent Code: #230063
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CAS Number 23235-03-2

science Other reagents with same CAS 23235-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 113.12 g/mol
Formula C₅H₇NO₂
thermostat Physical Properties
Boiling Point 272.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its alkyne functionality allows for click chemistry applications, particularly in drug discovery and development of peptide-based therapeutics. The primary amine and carboxylic acid groups enable coupling reactions for peptide synthesis. Frequently employed in research settings to probe enzyme mechanisms or design enzyme inhibitors due to its structural similarity to natural amino acids with added reactivity from the triple bond.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿400.00
inventory 5g
10-20 days ฿5,230.00
inventory 1g
10-20 days ฿1,050.00

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(R)-2-Aminopent-4-ynoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its alkyne functionality allows for click chemistry applications, particularly in drug discovery and development of peptide-based therapeutics. The primary amine and carboxylic acid groups enable coupling reactions for peptide synthesis. Frequently employed in research settings to probe enzyme mechanisms or design enzyme inhibitors due to its structural similarity to natural amino acids with added react

Used as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its alkyne functionality allows for click chemistry applications, particularly in drug discovery and development of peptide-based therapeutics. The primary amine and carboxylic acid groups enable coupling reactions for peptide synthesis. Frequently employed in research settings to probe enzyme mechanisms or design enzyme inhibitors due to its structural similarity to natural amino acids with added reactivity from the triple bond.

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