(S)-2-(Cyclohexylamino)propanoic acid

≥95%

Reagent Code: #50565
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CAS Number 82017-30-9

science Other reagents with same CAS 82017-30-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.24 g/mol
Formula C₉H₁₇NO₂
badge Registry Numbers
MDL Number MFCD16039417
thermostat Physical Properties
Boiling Point 296.8±23.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

(S)-2-(Cyclohexylamino)propanoic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the development of various biologically active compounds. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular diseases. Additionally, it is utilized in the preparation of peptidomimetics, which are compounds designed to mimic the structure and function of peptides, aiding in drug discovery and development. The compound is also explored in the study of enzyme inhibitors and receptor ligands, contributing to advancements in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿20,520.00
inventory 1g
10-20 days ฿7,839.00
inventory 250mg
10-20 days ฿3,915.00

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(S)-2-(Cyclohexylamino)propanoic acid
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(S)-2-(Cyclohexylamino)propanoic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the development of various biologically active compounds. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular diseases. Additionally, it is utilized in the preparation of peptidomimetics, which are compounds designed to mimic the structure and function

(S)-2-(Cyclohexylamino)propanoic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the development of various biologically active compounds. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular diseases. Additionally, it is utilized in the preparation of peptidomimetics, which are compounds designed to mimic the structure and function of peptides, aiding in drug discovery and development. The compound is also explored in the study of enzyme inhibitors and receptor ligands, contributing to advancements in medicinal chemistry.

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