(R)-2-Amino-2-cyclopentylacetic acid

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Reagent Code: #51112
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CAS Number 2521-86-0

science Other reagents with same CAS 2521-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.18 g/mol
Formula C₇H₁₃NO₂
badge Registry Numbers
MDL Number MFCD03788075
thermostat Physical Properties
Boiling Point 276.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

Used in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders. It serves as a chiral building block in organic chemistry, aiding in the creation of enantiomerically pure substances. Applied in research for designing enzyme inhibitors due to its structural similarity to natural amino acids. Also utilized in peptide synthesis to introduce specific cyclopentyl groups into peptide chains, enhancing their stability and biological activity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿63,954.00
inventory 250mg
10-20 days ฿6,543.00
inventory 1g
10-20 days ฿16,443.00

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(R)-2-Amino-2-cyclopentylacetic acid
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Used in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders. It serves as a chiral building block in organic chemistry, aiding in the creation of enantiomerically pure substances. Applied in research for designing enzyme inhibitors due to its structural similarity to natural amino acids. Also utilized in peptide synthesis to introduce specific cyclopentyl groups into peptide chains, enhancing their stability and biological activity.
Used in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders. It serves as a chiral building block in organic chemistry, aiding in the creation of enantiomerically pure substances. Applied in research for designing enzyme inhibitors due to its structural similarity to natural amino acids. Also utilized in peptide synthesis to introduce specific cyclopentyl groups into peptide chains, enhancing their stability and biological activity.
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