(S)-2-(Aminomethyl)-4-methylpentanoic acid

≥95%

Reagent Code: #38176
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CAS Number 203854-56-2

science Other reagents with same CAS 203854-56-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.20 g/mol
Formula C₇H₁₅NO₂
badge Registry Numbers
MDL Number MFCD07372884
thermostat Physical Properties
Boiling Point 249.1±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-(Aminomethyl)-4-methylpentanoic acid is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a building block in the development of drugs targeting neurological disorders, particularly those related to the central nervous system. Its structure allows it to act as a precursor for creating molecules with potential therapeutic effects, such as anticonvulsants or neuroprotective agents. Additionally, it is utilized in research to study enzyme interactions and metabolic pathways, aiding in the discovery of new treatments for various diseases. Its chiral nature makes it valuable in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,460.00
inventory 1g
10-20 days ฿65,990.00
inventory 250mg
10-20 days ฿26,380.00

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(S)-2-(Aminomethyl)-4-methylpentanoic acid
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(S)-2-(Aminomethyl)-4-methylpentanoic acid is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a building block in the development of drugs targeting neurological disorders, particularly those related to the central nervous system. Its structure allows it to act as a precursor for creating molecules with potential therapeutic effects, such as anticonvulsants or neuroprotective agents. Additionally, it is utilized in research to study enzyme interactions and metabolic pathways, aiding in the discovery of new treatments for various diseases. Its chiral nature makes it valuable in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
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