(R)-3-Amino-4-(o-tolyl)butanoic acid

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Reagent Code: #37618
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CAS Number 269398-79-0

science Other reagents with same CAS 269398-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.24 g/mol
Formula C₁₁H₁₅NO₂
badge Registry Numbers
MDL Number MFCD11870812
thermostat Physical Properties
Boiling Point 496.0±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

(R)-3-Amino-4-(o-tolyl)butanoic acid finds its primary application in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, such as epilepsy and Parkinson's disease, due to its structural similarity to gamma-aminobutyric acid (GABA), a crucial neurotransmitter. Additionally, this compound is utilized in the production of chiral molecules, where its stereochemistry plays a significant role in enhancing the efficacy and specificity of therapeutic agents. Its versatility also extends to research applications, where it serves as a building block for studying enzyme interactions and designing novel inhibitors for specific biochemical pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,850.00
inventory 100mg
10-20 days ฿2,925.00

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(R)-3-Amino-4-(o-tolyl)butanoic acid
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(R)-3-Amino-4-(o-tolyl)butanoic acid finds its primary application in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. It is particularly valuable in the development of drugs targeting neurological disorders, such as epilepsy and Parkinson's disease, due to its structural similarity to gamma-aminobutyric acid (GABA), a crucial neurotransmitter. Additionally, this compound is utilized in the production of chiral molecules, where its stereochemistry plays a significant role in enhancing the efficacy and specificity of therapeutic agents. Its versatility also extends to research applications, where it serves as a building block for studying enzyme interactions and designing novel inhibitors for specific biochemical pathways.
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